Canonical Allele Identifier: CA2260105477

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624249G= , CM000679.2:g.41624249G=	GRCh38
NC_000017.10:g.39780501G= , CM000679.1:g.39780501G=	GRCh37
NC_000017.9:g.37034027G=	NCBI36
NG_008625.1:g.5382C=
NG_009090.2:g.167464C= , LRG_401:g.167464C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.261C= MANE Select	ENSP00000308452.8:p.Thr87=
ENST00000311208.12:c.261C=	ENSP00000308452.8:p.Thr87=
ENST00000463128.5:c.-312-43C=	ENSP00000468672.1:n.-312-43C=
ENST00000491673.1:n.327C=
ENST00000493253.5:n.48C=
ENST00000540235.5:c.56C=	ENSP00000441751.2:p.Pro19=
ENST00000577817.3:c.216C=	ENSP00000467418.1:p.Thr72=
NM_000422.2:c.261C=	NP_000413.1:p.Thr87=
NM_000422.3:c.261C= MANE Select	NP_000413.1:p.Thr87=