Canonical Allele Identifier: CA399389200
Gene: KRT12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866994A>T , CM000679.2:g.40866994A>T GRCh38
NC_000017.10:g.39023246A>T , CM000679.1:g.39023246A>T GRCh37
NC_000017.9:g.36276772A>T NCBI36
NG_008077.1:g.5217T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.193T>A MANE Select ENSP00000251643.4:p.Ser65Thr
ENST00000647902.1:c.193T>A ENSP00000497770.1:p.Ser65Thr
ENST00000251643.4:c.193T>A ENSP00000251643.4:p.Ser65Thr
NM_000223.3:c.193T>A NP_000214.1:p.Ser65Thr
XR_934754.1:n.1500+16134A>T
XR_934754.2:n.2008+16134A>T
NM_000223.4:c.193T>A MANE Select NP_000214.1:p.Ser65Thr