Canonical Allele Identifier: CA384991373

Gene: KRT4

Linked Data

• MyVariant Identifiers: chr12:g.53207797T>A (hg19) ; chr12:g.52814013T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814013T>A , CM000674.2:g.52814013T>A	GRCh38
NC_000012.11:g.53207797T>A , CM000674.1:g.53207797T>A	GRCh37
NC_000012.10:g.51494064T>A	NCBI36
NG_007380.1:g.5539A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.2:c.46A>T MANE Select	ENSP00000448220.1:p.Ser16Cys
ENST00000548097.5:c.46A>T	ENSP00000449755.1:p.Ser16Cys
ENST00000551956.1:c.46A>T	ENSP00000448220.1:p.Ser16Cys
ENST00000552668.1:c.46A>T	ENSP00000447320.1:p.Ser16Cys
NM_002272.3:c.46A>T	NP_002263.3:p.Ser16Cys
NM_002272.4:c.46A>T MANE Select	NP_002263.3:p.Ser16Cys