Canonical Allele Identifier: CA479873815
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53203179G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809395G>T , CM000674.2:g.52809395G>T GRCh38
NC_000012.11:g.53203179G>T , CM000674.1:g.53203179G>T GRCh37
NC_000012.10:g.51489446G>T NCBI36
NG_007380.1:g.10157C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.822C>A MANE Select ENSP00000448220.1:p.Val274=
ENST00000548097.5:c.*334C>A ENSP00000449755.1:n.*334C>A
ENST00000549295.1:n.256C>A
ENST00000551956.1:c.822C>A ENSP00000448220.1:p.Val274=
ENST00000552668.1:c.*227C>A ENSP00000447320.1:n.*227C>A
NM_002272.3:c.822C>A NP_002263.3:p.Val274=
NM_002272.4:c.822C>A MANE Select NP_002263.3:p.Val274=
Search 100 bp 5'
Search 100 bp 3'