Canonical Allele Identifier: CA399389145
Gene: KRT12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866981A>C , CM000679.2:g.40866981A>C GRCh38
NC_000017.10:g.39023233A>C , CM000679.1:g.39023233A>C GRCh37
NC_000017.9:g.36276759A>C NCBI36
NG_008077.1:g.5230T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.206T>G MANE Select ENSP00000251643.4:p.Phe69Cys
ENST00000647902.1:c.206T>G ENSP00000497770.1:p.Phe69Cys
ENST00000251643.4:c.206T>G ENSP00000251643.4:p.Phe69Cys
NM_000223.3:c.206T>G NP_000214.1:p.Phe69Cys
XR_934754.1:n.1500+16121A>C
XR_934754.2:n.2008+16121A>C
NM_000223.4:c.206T>G MANE Select NP_000214.1:p.Phe69Cys