Canonical Allele Identifier: CA399389354
Gene: KRT12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867038C>G , CM000679.2:g.40867038C>G GRCh38
NC_000017.10:g.39023290C>G , CM000679.1:g.39023290C>G GRCh37
NC_000017.9:g.36276816C>G NCBI36
NG_008077.1:g.5173G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.149G>C MANE Select ENSP00000251643.4:p.Gly50Ala
ENST00000647902.1:c.149G>C ENSP00000497770.1:p.Gly50Ala
ENST00000251643.4:c.149G>C ENSP00000251643.4:p.Gly50Ala
NM_000223.3:c.149G>C NP_000214.1:p.Gly50Ala
XR_934754.1:n.1500+16178C>G
XR_934754.2:n.2008+16178C>G
NM_000223.4:c.149G>C MANE Select NP_000214.1:p.Gly50Ala