Canonical Allele Identifier: CA7115838
Community Standard Title: NM_002471.4(MYH6):c.1327C>T (p.Arg443Cys)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23400792G>A , CM000676.2:g.23400792G>A GRCh38
NC_000014.8:g.23870001G>A , CM000676.1:g.23870001G>A GRCh37
NC_000014.7:g.22939841G>A NCBI36
NG_023444.1:g.12486C>T , LRG_389:g.12486C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.1327C>T MANE Select NP_002462.2:p.Arg443Cys
ENST00000405093.9:c.1327C>T MANE Select ENSP00000386041.3:p.Arg443Cys
NM_002471.3:c.1327C>T , LRG_389t1:c.1327C>T NP_002462.2:p.Arg443Cys
ENST00000356287.3:c.1327C>T ENSP00000348634.3:p.Arg443Cys
ENST00000405093.7:c.1327C>T ENSP00000386041.3:p.Arg443Cys
ENST00000557461.1:n.1381C>T
ENST00000557461.2:n.1394C>T