Canonical Allele Identifier: CA2259745887

Gene: KRT12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866936C= , CM000679.2:g.40866936C=	GRCh38
NC_000017.10:g.39023188C= , CM000679.1:g.39023188C=	GRCh37
NC_000017.9:g.36276714C=	NCBI36
NG_008077.1:g.5275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.251G= MANE Select	ENSP00000251643.4:p.Gly84=
ENST00000647902.1:c.211+40G=	ENSP00000497770.1:n.211+40G=
ENST00000251643.4:c.251G=	ENSP00000251643.4:p.Gly84=
NM_000223.3:c.251G=	NP_000214.1:p.Gly84=
XR_934754.1:n.1500+16076C=
XR_934754.2:n.2008+16076C=
NM_000223.4:c.251G= MANE Select	NP_000214.1:p.Gly84=