Canonical Allele Identifier: CA485766562

Linked Data

MyVariant Identifiers: chr14:g.23885395G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416186G>A , CM000676.2:g.23416186G>A GRCh38
NC_000014.8:g.23885395G>A , CM000676.1:g.23885395G>A GRCh37
NC_000014.7:g.22955235G>A NCBI36
NG_007884.1:g.24476C>T , LRG_384:g.24476C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4771C>T (MYH7) MANE Select ENSP00000347507.3:p.Leu1591=
ENST00000355349.3:c.4771C>T (MYH7) ENSP00000347507.3:p.Leu1591=
NM_000257.3:c.4771C>T (MYH7) NP_000248.2:p.Leu1591=
NR_126491.1:n.447G>A (MHRT)
XM_017021340.1:c.4771C>T (MYH7) XP_016876829.1:p.Leu1591=
NM_000257.4:c.4771C>T (MYH7) MANE Select NP_000248.2:p.Leu1591=