Canonical Allele Identifier: CA384991339

Gene: KRT4

Linked Data

• MyVariant Identifiers: chr12:g.53207779C>G (hg19) ; chr12:g.52813995C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52813995C>G , CM000674.2:g.52813995C>G	GRCh38
NC_000012.11:g.53207779C>G , CM000674.1:g.53207779C>G	GRCh37
NC_000012.10:g.51494046C>G	NCBI36
NG_007380.1:g.5557G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.2:c.64G>C MANE Select	ENSP00000448220.1:p.Val22Leu
ENST00000548097.5:c.64G>C	ENSP00000449755.1:p.Val22Leu
ENST00000551956.1:c.64G>C	ENSP00000448220.1:p.Val22Leu
ENST00000552668.1:c.64G>C	ENSP00000447320.1:p.Val22Leu
NM_002272.3:c.64G>C	NP_002263.3:p.Val22Leu
NM_002272.4:c.64G>C MANE Select	NP_002263.3:p.Val22Leu