Canonical Allele Identifier: CA2036689836
Gene: KRT4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809418C= , CM000674.2:g.52809418C= GRCh38
NC_000012.11:g.53203202C= , CM000674.1:g.53203202C= GRCh37
NC_000012.10:g.51489469C= NCBI36
NG_007380.1:g.10134G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.799G= MANE Select ENSP00000448220.1:p.Asp267=
ENST00000548097.5:c.*311G= ENSP00000449755.1:n.*311G=
ENST00000549295.1:n.233G=
ENST00000551956.1:c.799G= ENSP00000448220.1:p.Asp267=
ENST00000552668.1:c.*204G= ENSP00000447320.1:n.*204G=
NM_002272.3:c.799G= NP_002263.3:p.Asp267=
NM_002272.4:c.799G= MANE Select NP_002263.3:p.Asp267=
Search 100 bp 5'
Search 100 bp 3'