Canonical Allele Identifier: CA399389067
Gene: KRT12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866961A>G , CM000679.2:g.40866961A>G GRCh38
NC_000017.10:g.39023213A>G , CM000679.1:g.39023213A>G GRCh37
NC_000017.9:g.36276739A>G NCBI36
NG_008077.1:g.5250T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.226T>C MANE Select ENSP00000251643.4:p.Ser76Pro
ENST00000647902.1:c.211+15T>C ENSP00000497770.1:n.211+15T>C
ENST00000251643.4:c.226T>C ENSP00000251643.4:p.Ser76Pro
NM_000223.3:c.226T>C NP_000214.1:p.Ser76Pro
XR_934754.1:n.1500+16101A>G
XR_934754.2:n.2008+16101A>G
NM_000223.4:c.226T>C MANE Select NP_000214.1:p.Ser76Pro