Canonical Allele Identifier: CA2260105540

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624359T= , CM000679.2:g.41624359T=	GRCh38
NC_000017.10:g.39780611T= , CM000679.1:g.39780611T=	GRCh37
NC_000017.9:g.37034137T=	NCBI36
NG_008625.1:g.5272A=
NG_009090.2:g.167354A= , LRG_401:g.167354A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.151A= MANE Select	ENSP00000308452.8:p.Thr51=
ENST00000311208.12:c.151A=	ENSP00000308452.8:p.Thr51=
ENST00000463128.5:c.-312-153A=	ENSP00000468672.1:n.-312-153A=
ENST00000491673.1:n.217A=
ENST00000540235.5:c.-55A=	ENSP00000441751.2:n.-55A=
ENST00000577817.3:c.106A=	ENSP00000467418.1:p.Thr36=
NM_000422.2:c.151A=	NP_000413.1:p.Thr51=
NM_000422.3:c.151A= MANE Select	NP_000413.1:p.Thr51=