Canonical Allele Identifier: CA389037129

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415769T>G , CM000676.2:g.23415769T>G GRCh38
NC_000014.8:g.23884978T>G , CM000676.1:g.23884978T>G GRCh37
NC_000014.7:g.22954818T>G NCBI36
NG_007884.1:g.24893A>C , LRG_384:g.24893A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5017A>C (MYH7) MANE Select ENSP00000347507.3:p.Ile1673Leu
ENST00000355349.3:c.5017A>C (MYH7) ENSP00000347507.3:p.Ile1673Leu
NM_000257.3:c.5017A>C (MYH7) NP_000248.2:p.Ile1673Leu
NR_126491.1:n.201T>G (MHRT)
XM_017021340.1:c.5017A>C (MYH7) XP_016876829.1:p.Ile1673Leu
NM_000257.4:c.5017A>C (MYH7) MANE Select NP_000248.2:p.Ile1673Leu