Canonical Allele Identifier: CA2260105594

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624444G= , CM000679.2:g.41624444G=	GRCh38
NC_000017.10:g.39780696G= , CM000679.1:g.39780696G=	GRCh37
NC_000017.9:g.37034222G=	NCBI36
NG_008625.1:g.5187C=
NG_009090.2:g.167269C= , LRG_401:g.167269C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.66C= MANE Select	ENSP00000308452.8:p.Gly22=
ENST00000311208.12:c.66C=	ENSP00000308452.8:p.Gly22=
ENST00000463128.5:c.-312-238C=	ENSP00000468672.1:n.-312-238C=
ENST00000491673.1:n.132C=
ENST00000540235.5:c.-140C=	ENSP00000441751.2:n.-140C=
ENST00000577817.3:c.21C=	ENSP00000467418.1:p.Gly7=
NM_000422.2:c.66C=	NP_000413.1:p.Gly22=
NM_000422.3:c.66C= MANE Select	NP_000413.1:p.Gly22=