Canonical Allele Identifier: CA2260105596

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624445C= , CM000679.2:g.41624445C=	GRCh38
NC_000017.10:g.39780697C= , CM000679.1:g.39780697C=	GRCh37
NC_000017.9:g.37034223C=	NCBI36
NG_008625.1:g.5186G=
NG_009090.2:g.167268G= , LRG_401:g.167268G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.65G= MANE Select	ENSP00000308452.8:p.Gly22=
ENST00000311208.12:c.65G=	ENSP00000308452.8:p.Gly22=
ENST00000463128.5:c.-312-239G=	ENSP00000468672.1:n.-312-239G=
ENST00000491673.1:n.131G=
ENST00000540235.5:c.-141G=	ENSP00000441751.2:n.-141G=
ENST00000577817.3:c.20G=	ENSP00000467418.1:p.Gly7=
NM_000422.2:c.65G=	NP_000413.1:p.Gly22=
NM_000422.3:c.65G= MANE Select	NP_000413.1:p.Gly22=