Canonical Allele Identifier: CA2036663516
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813940C= , CM000674.2:g.52813940C= GRCh38
NC_000012.11:g.53207724C= , CM000674.1:g.53207724C= GRCh37
NC_000012.10:g.51493991C= NCBI36
NG_007380.1:g.5612G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.119G= MANE Select ENSP00000448220.1:p.Gly40=
ENST00000548097.5:c.119G= ENSP00000449755.1:p.Gly40=
ENST00000551956.1:c.119G= ENSP00000448220.1:p.Gly40=
ENST00000552668.1:c.119G= ENSP00000447320.1:p.Gly40=
NM_002272.3:c.119G= NP_002263.3:p.Gly40=
NM_002272.4:c.119G= MANE Select NP_002263.3:p.Gly40=