Canonical Allele Identifier: CA2036663514
Gene: KRT4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.122G= MANE Select ENSP00000448220.1:p.Arg41=
ENST00000548097.5:c.122G= ENSP00000449755.1:p.Arg41=
ENST00000551956.1:c.122G= ENSP00000448220.1:p.Arg41=
ENST00000552668.1:c.122G= ENSP00000447320.1:p.Arg41=
NM_002272.3:c.122G= NP_002263.3:p.Arg41=
NM_002272.4:c.122G= MANE Select NP_002263.3:p.Arg41=