Canonical Allele Identifier: CA485766439

Linked Data

MyVariant Identifiers: chr14:g.23885479G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416270G>A , CM000676.2:g.23416270G>A GRCh38
NC_000014.8:g.23885479G>A , CM000676.1:g.23885479G>A GRCh37
NC_000014.7:g.22955319G>A NCBI36
NG_007884.1:g.24392C>T , LRG_384:g.24392C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4687C>T (MYH7) MANE Select ENSP00000347507.3:p.Leu1563=
ENST00000355349.3:c.4687C>T (MYH7) ENSP00000347507.3:p.Leu1563=
NM_000257.3:c.4687C>T (MYH7) NP_000248.2:p.Leu1563=
NR_126491.1:n.531G>A (MHRT)
XM_017021340.1:c.4687C>T (MYH7) XP_016876829.1:p.Leu1563=
NM_000257.4:c.4687C>T (MYH7) MANE Select NP_000248.2:p.Leu1563=