Canonical Allele Identifier: CA2199825576

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048897G= , CM000677.2:g.100048897G=	GRCh38
NC_000015.9:g.100589102G= , CM000677.1:g.100589102G=	GRCh37
NC_000015.8:g.98406625G=	NCBI36
NG_016287.1:g.298082C=
NG_016287.2:g.298082C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2551C= MANE Select	ENSP00000268070.4:p.Pro851=
ENST00000568565.2:c.2632C=	ENSP00000456161.2:p.Pro878=
ENST00000268070.8:c.2551C=	ENSP00000268070.4:p.Pro851=
NM_139057.2:c.2551C=	NP_620688.2:p.Pro851=
XM_005254872.2:c.2632C=	XP_005254929.1:p.Pro878=
XM_011521312.1:c.2701C=	XP_011519614.1:p.Pro901=
NM_139057.3:c.2551C=	NP_620688.2:p.Pro851=
XM_005254872.3:c.2632C=	XP_005254929.1:p.Pro878=
XM_011521312.2:c.2701C=	XP_011519614.1:p.Pro901=
XM_017021973.2:c.2833C=	XP_016877462.1:p.Pro945=
XM_017021974.1:c.2833C=	XP_016877463.1:p.Pro945=
XM_017021975.1:c.2764C=	XP_016877464.1:p.Pro922=
XM_017021976.1:c.2104C=	XP_016877465.1:p.Pro702=
XM_017021978.1:c.1735C=	XP_016877467.1:p.Pro579=
XM_017021979.1:c.1513C=	XP_016877468.1:p.Pro505=
XM_017021980.1:c.1513C=	XP_016877469.1:p.Pro505=
XM_017021982.1:c.1222C=	XP_016877471.1:p.Pro408=
XM_017021983.1:c.1006C=	XP_016877472.1:p.Pro336=
NM_139057.4:c.2551C= MANE Select	NP_620688.2:p.Pro851=