Canonical Allele Identifier: CA2199825630

Gene: ADAMTS17

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100049012G= , CM000677.2:g.100049012G=	GRCh38
NC_000015.9:g.100589217G= , CM000677.1:g.100589217G=	GRCh37
NC_000015.8:g.98406740G=	NCBI36
NG_016287.1:g.297967C=
NG_016287.2:g.297967C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2456-20C= MANE Select	ENSP00000268070.4:n.2456-20C=
ENST00000568565.2:c.2537-20C=	ENSP00000456161.2:n.2537-20C=
ENST00000268070.8:c.2456-20C=	ENSP00000268070.4:n.2456-20C=
NM_139057.2:c.2456-20C=	NP_620688.2:n.2456-20C=
XM_005254872.2:c.2537-20C=	XP_005254929.1:n.2537-20C=
XM_011521312.1:c.2606-20C=	XP_011519614.1:n.2606-20C=
NM_139057.3:c.2456-20C=	NP_620688.2:n.2456-20C=
XM_005254872.3:c.2537-20C=	XP_005254929.1:n.2537-20C=
XM_011521312.2:c.2606-20C=	XP_011519614.1:n.2606-20C=
XM_017021973.2:c.2738-20C=	XP_016877462.1:n.2738-20C=
XM_017021974.1:c.2738-20C=	XP_016877463.1:n.2738-20C=
XM_017021975.1:c.2669-20C=	XP_016877464.1:n.2669-20C=
XM_017021976.1:c.2009-20C=	XP_016877465.1:n.2009-20C=
XM_017021978.1:c.1640-20C=	XP_016877467.1:n.1640-20C=
XM_017021979.1:c.1418-20C=	XP_016877468.1:n.1418-20C=
XM_017021980.1:c.1418-20C=	XP_016877469.1:n.1418-20C=
XM_017021982.1:c.1127-20C=	XP_016877471.1:n.1127-20C=
XM_017021983.1:c.911-20C=	XP_016877472.1:n.911-20C=
NM_139057.4:c.2456-20C= MANE Select	NP_620688.2:n.2456-20C=