Canonical Allele Identifier: CA480075644
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53201484C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52807700C>A , CM000674.2:g.52807700C>A GRCh38
NC_000012.11:g.53201484C>A , CM000674.1:g.53201484C>A GRCh37
NC_000012.10:g.51487751C>A NCBI36
NG_007380.1:g.11852G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.1290G>T MANE Select ENSP00000448220.1:p.Leu430=
ENST00000548097.5:c.*802G>T ENSP00000449755.1:n.*802G>T
ENST00000551956.1:c.1290G>T ENSP00000448220.1:p.Leu430=
NM_002272.3:c.1290G>T NP_002263.3:p.Leu430=
NM_002272.4:c.1290G>T MANE Select NP_002263.3:p.Leu430=
Search 100 bp 5'
Search 100 bp 3'