Canonical Allele Identifier: CA405684156
Gene: RYR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39068564G>A (hg19) chr19:g.38577924G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38577924G>A , CM000681.2:g.38577924G>A GRCh38
NC_000019.9:g.39068564G>A , CM000681.1:g.39068564G>A GRCh37
NC_000019.8:g.43760404G>A NCBI36
NG_008866.1:g.149225G>A , LRG_766:g.149225G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593677.2:c.1115G>A
ENST00000688602.1:c.2512G>A
ENST00000689936.1:c.2484G>A
ENST00000359596.8:c.14179G>A MANE Select ENSP00000352608.2:p.Asp4727Asn
ENST00000355481.8:c.14164G>A ENSP00000347667.3:p.Asp4722Asn
ENST00000359596.7:c.14179G>A ENSP00000352608.2:p.Asp4727Asn
ENST00000360985.7:c.14161G>A ENSP00000354254.4:p.Asp4721Asn
NM_000540.2:c.14179G>A , LRG_766t1:c.14179G>A NP_000531.2:p.Asp4727Asn
NM_001042723.1:c.14164G>A NP_001036188.1:p.Asp4722Asn
XM_006723317.1:c.14161G>A XP_006723380.1:p.Asp4721Asn
XM_006723319.1:c.14146G>A XP_006723382.1:p.Asp4716Asn
XM_011527204.1:c.14176G>A XP_011525506.1:p.Asp4726Asn
XM_011527205.1:c.14092G>A XP_011525507.1:p.Asp4698Asn
XM_006723317.2:c.14161G>A XP_006723380.1:p.Asp4721Asn
XM_006723319.2:c.14146G>A XP_006723382.1:p.Asp4716Asn
XM_011527205.2:c.14092G>A XP_011525507.1:p.Asp4698Asn
NM_000540.3:c.14179G>A MANE Select NP_000531.2:p.Asp4727Asn
NM_001042723.2:c.14164G>A NP_001036188.1:p.Asp4722Asn
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