Canonical Allele Identifier: CA2259745961
Gene: KRT12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867117G= , CM000679.2:g.40867117G= GRCh38
NC_000017.10:g.39023369G= , CM000679.1:g.39023369G= GRCh37
NC_000017.9:g.36276895G= NCBI36
NG_008077.1:g.5094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.70C= MANE Select ENSP00000251643.4:p.Gln24=
ENST00000647902.1:c.70C= ENSP00000497770.1:p.Gln24=
ENST00000251643.4:c.70C= ENSP00000251643.4:p.Gln24=
NM_000223.3:c.70C= NP_000214.1:p.Gln24=
XR_934754.1:n.1500+16257G=
XR_934754.2:n.2008+16257G=
NM_000223.4:c.70C= MANE Select NP_000214.1:p.Gln24=