Canonical Allele Identifier: CA389037610

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416158G>T , CM000676.2:g.23416158G>T GRCh38
NC_000014.8:g.23885367G>T , CM000676.1:g.23885367G>T GRCh37
NC_000014.7:g.22955207G>T NCBI36
NG_007884.1:g.24504C>A , LRG_384:g.24504C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4799C>A (MYH7) MANE Select ENSP00000347507.3:p.Ser1600Tyr
ENST00000355349.3:c.4799C>A (MYH7) ENSP00000347507.3:p.Ser1600Tyr
NM_000257.3:c.4799C>A (MYH7) NP_000248.2:p.Ser1600Tyr
NR_126491.1:n.419G>T (MHRT)
XM_017021340.1:c.4799C>A (MYH7) XP_016876829.1:p.Ser1600Tyr
NM_000257.4:c.4799C>A (MYH7) MANE Select NP_000248.2:p.Ser1600Tyr