Canonical Allele Identifier: CA480076156
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53207720T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813936T>A , CM000674.2:g.52813936T>A GRCh38
NC_000012.11:g.53207720T>A , CM000674.1:g.53207720T>A GRCh37
NC_000012.10:g.51493987T>A NCBI36
NG_007380.1:g.5616A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.123A>T MANE Select ENSP00000448220.1:p.Arg41=
ENST00000548097.5:c.123A>T ENSP00000449755.1:p.Arg41=
ENST00000551956.1:c.123A>T ENSP00000448220.1:p.Arg41=
ENST00000552668.1:c.123A>T ENSP00000447320.1:p.Arg41=
NM_002272.3:c.123A>T NP_002263.3:p.Arg41=
NM_002272.4:c.123A>T MANE Select NP_002263.3:p.Arg41=