Canonical Allele Identifier: CA399389859
Gene: KRT12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867147T>C , CM000679.2:g.40867147T>C GRCh38
NC_000017.10:g.39023399T>C , CM000679.1:g.39023399T>C GRCh37
NC_000017.9:g.36276925T>C NCBI36
NG_008077.1:g.5064A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.40A>G MANE Select ENSP00000251643.4:p.Thr14Ala
ENST00000647902.1:c.40A>G ENSP00000497770.1:p.Thr14Ala
ENST00000251643.4:c.40A>G ENSP00000251643.4:p.Thr14Ala
NM_000223.3:c.40A>G NP_000214.1:p.Thr14Ala
XR_934754.1:n.1500+16287T>C
XR_934754.2:n.2008+16287T>C
NM_000223.4:c.40A>G MANE Select NP_000214.1:p.Thr14Ala