Canonical Allele Identifier: CA384985768
Gene: KRT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52807687C>A , CM000674.2:g.52807687C>A GRCh38
NC_000012.11:g.53201471C>A , CM000674.1:g.53201471C>A GRCh37
NC_000012.10:g.51487738C>A NCBI36
NG_007380.1:g.11865G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.1303G>T MANE Select ENSP00000448220.1:p.Glu435Ter
ENST00000548097.5:c.*815G>T ENSP00000449755.1:n.*815G>T
ENST00000551956.1:c.1303G>T ENSP00000448220.1:p.Glu435Ter
NM_002272.3:c.1303G>T NP_002263.3:p.Glu435Ter
NM_002272.4:c.1303G>T MANE Select NP_002263.3:p.Glu435Ter