Canonical Allele Identifier: CA275531652

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs4965593
• MyVariant Identifiers: chr15:g.100758385C>T (hg19) ; chr15:g.100218180C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100218180C>T , CM000677.2:g.100218180C>T	GRCh38
NC_000015.9:g.100758385C>T , CM000677.1:g.100758385C>T	GRCh37
NC_000015.8:g.98575908C>T	NCBI36
NG_016287.1:g.128799G>A
NG_016287.2:g.128799G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000268070.9:c.1076-18757G>A MANE Select	ENSP00000268070.4:n.1076-18757G>A
ENST00000568565.2:c.1076-18757G>A	ENSP00000456161.2:n.1076-18757G>A
ENST00000268070.8:c.1076-18757G>A	ENSP00000268070.4:n.1076-18757G>A
ENST00000378898.8:n.757-18757G>A
ENST00000559976.1:n.72-18757G>A
NM_139057.2:c.1076-18757G>A	NP_620688.2:n.1076-18757G>A
XM_005254872.2:c.1076-18757G>A	XP_005254929.1:n.1076-18757G>A
XM_011521312.1:c.1076-18757G>A	XP_011519614.1:n.1076-18757G>A
NM_139057.3:c.1076-18757G>A	NP_620688.2:n.1076-18757G>A
XM_005254872.3:c.1076-18757G>A	XP_005254929.1:n.1076-18757G>A
XM_011521312.2:c.1076-18757G>A	XP_011519614.1:n.1076-18757G>A
XM_017021973.2:c.1207+17442G>A	XP_016877462.1:n.1207+17442G>A
XM_017021974.1:c.1207+17442G>A	XP_016877463.1:n.1207+17442G>A
XM_017021975.1:c.1207+17442G>A	XP_016877464.1:n.1207+17442G>A
XM_017021976.1:c.478+17442G>A	XP_016877465.1:n.478+17442G>A
XM_017021977.1:c.1207+17442G>A	XP_016877466.1:n.1207+17442G>A
XM_017021978.1:c.109+2053G>A	XP_016877467.1:n.109+2053G>A
XM_017021979.1:c.-8+35956G>A	XP_016877468.1:n.-8+35956G>A
XM_017021981.1:c.1207+17442G>A	XP_016877470.1:n.1207+17442G>A
XM_017021984.1:c.347-18757G>A	XP_016877473.1:n.347-18757G>A
XR_001751118.1:n.2229+17442G>A
XR_001751119.1:n.2229+17442G>A
XR_001751120.1:n.2229+17442G>A
NM_139057.4:c.1076-18757G>A MANE Select	NP_620688.2:n.1076-18757G>A