Canonical Allele Identifier: CA384991223
Gene: KRT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813937C>G , CM000674.2:g.52813937C>G GRCh38
NC_000012.11:g.53207721C>G , CM000674.1:g.53207721C>G GRCh37
NC_000012.10:g.51493988C>G NCBI36
NG_007380.1:g.5615G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.122G>C MANE Select ENSP00000448220.1:p.Arg41Pro
ENST00000548097.5:c.122G>C ENSP00000449755.1:p.Arg41Pro
ENST00000551956.1:c.122G>C ENSP00000448220.1:p.Arg41Pro
ENST00000552668.1:c.122G>C ENSP00000447320.1:p.Arg41Pro
NM_002272.3:c.122G>C NP_002263.3:p.Arg41Pro
NM_002272.4:c.122G>C MANE Select NP_002263.3:p.Arg41Pro