Canonical Allele Identifier: CA384988697
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1325693530
MyVariant Identifiers: chr12:g.53203250C>A (hg19) chr12:g.52809466C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809466C>A , CM000674.2:g.52809466C>A GRCh38
NC_000012.11:g.53203250C>A , CM000674.1:g.53203250C>A GRCh37
NC_000012.10:g.51489517C>A NCBI36
NG_007380.1:g.10086G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.751G>T MANE Select ENSP00000448220.1:p.Ala251Ser
ENST00000548097.5:c.*263G>T ENSP00000449755.1:n.*263G>T
ENST00000549295.1:n.185G>T
ENST00000551956.1:c.751G>T ENSP00000448220.1:p.Ala251Ser
ENST00000552668.1:c.*156G>T ENSP00000447320.1:n.*156G>T
NM_002272.3:c.751G>T NP_002263.3:p.Ala251Ser
NM_002272.4:c.751G>T MANE Select NP_002263.3:p.Ala251Ser
Search 100 bp 5'
Search 100 bp 3'