Canonical Allele Identifier: CA2036689012
Gene: KRT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52807692T= , CM000674.2:g.52807692T= GRCh38
NC_000012.11:g.53201476T= , CM000674.1:g.53201476T= GRCh37
NC_000012.10:g.51487743T= NCBI36
NG_007380.1:g.11860A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.1298A= MANE Select ENSP00000448220.1:p.Asp433=
ENST00000548097.5:c.*810A= ENSP00000449755.1:n.*810A=
ENST00000551956.1:c.1298A= ENSP00000448220.1:p.Asp433=
NM_002272.3:c.1298A= NP_002263.3:p.Asp433=
NM_002272.4:c.1298A= MANE Select NP_002263.3:p.Asp433=