Canonical Allele Identifier: CA405692515
Community Standard Title: NM_000540.3(RYR1):c.14863A>C (p.Met4955Leu)
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38585997A>C , CM000681.2:g.38585997A>C GRCh38
NC_000019.9:g.39076637A>C , CM000681.1:g.39076637A>C GRCh37
NC_000019.8:g.43768477A>C NCBI36
NG_008866.1:g.157298A>C , LRG_766:g.157298A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000540.3:c.14863A>C MANE Select NP_000531.2:p.Met4955Leu
ENST00000359596.8:c.14863A>C MANE Select ENSP00000352608.2:p.Met4955Leu
NM_000540.2:c.14863A>C , LRG_766t1:c.14863A>C NP_000531.2:p.Met4955Leu
NM_001042723.1:c.14848A>C NP_001036188.1:p.Met4950Leu
NM_001042723.2:c.14848A>C NP_001036188.1:p.Met4950Leu
ENST00000355481.8:c.14848A>C ENSP00000347667.3:p.Met4950Leu
ENST00000359596.7:c.14863A>C ENSP00000352608.2:p.Met4955Leu
ENST00000360985.7:c.14845A>C ENSP00000354254.4:p.Met4949Leu
ENST00000593677.2:c.1799A>C
ENST00000688602.1:c.3196A>C
ENST00000689936.1:c.3168A>C
ENST00000692547.1:n.256A>C
XM_006723317.1:c.14845A>C XP_006723380.1:p.Met4949Leu
XM_006723317.2:c.14845A>C XP_006723380.1:p.Met4949Leu
XM_006723319.1:c.14830A>C XP_006723382.1:p.Met4944Leu
XM_006723319.2:c.14830A>C XP_006723382.1:p.Met4944Leu
XM_011527204.1:c.14860A>C XP_011525506.1:p.Met4954Leu
XM_011527205.1:c.14776A>C XP_011525507.1:p.Met4926Leu
XM_011527205.2:c.14776A>C XP_011525507.1:p.Met4926Leu