Canonical Allele Identifier: CA384991232
Gene: KRT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813943G>C , CM000674.2:g.52813943G>C GRCh38
NC_000012.11:g.53207727G>C , CM000674.1:g.53207727G>C GRCh37
NC_000012.10:g.51493994G>C NCBI36
NG_007380.1:g.5609C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.116C>G MANE Select ENSP00000448220.1:p.Ala39Gly
ENST00000548097.5:c.116C>G ENSP00000449755.1:p.Ala39Gly
ENST00000551956.1:c.116C>G ENSP00000448220.1:p.Ala39Gly
ENST00000552668.1:c.116C>G ENSP00000447320.1:p.Ala39Gly
NM_002272.3:c.116C>G NP_002263.3:p.Ala39Gly
NM_002272.4:c.116C>G MANE Select NP_002263.3:p.Ala39Gly