Canonical Allele Identifier: CA2036663564
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814042T= , CM000674.2:g.52814042T= GRCh38
NC_000012.11:g.53207826T= , CM000674.1:g.53207826T= GRCh37
NC_000012.10:g.51494093T= NCBI36
NG_007380.1:g.5510A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.17A= MANE Select ENSP00000448220.1:p.Gln6=
ENST00000548097.5:c.17A= ENSP00000449755.1:p.Gln6=
ENST00000551956.1:c.17A= ENSP00000448220.1:p.Gln6=
ENST00000552668.1:c.17A= ENSP00000447320.1:p.Gln6=
NM_002272.3:c.17A= NP_002263.3:p.Gln6=
NM_002272.4:c.17A= MANE Select NP_002263.3:p.Gln6=