Canonical Allele Identifier: CA2260105503

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624287C= , CM000679.2:g.41624287C=	GRCh38
NC_000017.10:g.39780539C= , CM000679.1:g.39780539C=	GRCh37
NC_000017.9:g.37034065C=	NCBI36
NG_008625.1:g.5344G=
NG_009090.2:g.167426G= , LRG_401:g.167426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.223G= MANE Select	ENSP00000308452.8:p.Gly75=
ENST00000311208.12:c.223G=	ENSP00000308452.8:p.Gly75=
ENST00000463128.5:c.-312-81G=	ENSP00000468672.1:n.-312-81G=
ENST00000491673.1:n.289G=
ENST00000493253.5:n.10G=
ENST00000540235.5:c.18G=	ENSP00000441751.2:p.Gly6=
ENST00000577817.3:c.178G=	ENSP00000467418.1:p.Gly60=
NM_000422.2:c.223G=	NP_000413.1:p.Gly75=
NM_000422.3:c.223G= MANE Select	NP_000413.1:p.Gly75=