Canonical Allele Identifier: CA393692384

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589104T>G (hg19) ; chr15:g.100048899T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048899T>G , CM000677.2:g.100048899T>G	GRCh38
NC_000015.9:g.100589104T>G , CM000677.1:g.100589104T>G	GRCh37
NC_000015.8:g.98406627T>G	NCBI36
NG_016287.1:g.298080A>C
NG_016287.2:g.298080A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2549A>C MANE Select	ENSP00000268070.4:p.Glu850Ala
ENST00000568565.2:c.2630A>C	ENSP00000456161.2:p.Glu877Ala
ENST00000268070.8:c.2549A>C	ENSP00000268070.4:p.Glu850Ala
NM_139057.2:c.2549A>C	NP_620688.2:p.Glu850Ala
XM_005254872.2:c.2630A>C	XP_005254929.1:p.Glu877Ala
XM_011521312.1:c.2699A>C	XP_011519614.1:p.Glu900Ala
NM_139057.3:c.2549A>C	NP_620688.2:p.Glu850Ala
XM_005254872.3:c.2630A>C	XP_005254929.1:p.Glu877Ala
XM_011521312.2:c.2699A>C	XP_011519614.1:p.Glu900Ala
XM_017021973.2:c.2831A>C	XP_016877462.1:p.Glu944Ala
XM_017021974.1:c.2831A>C	XP_016877463.1:p.Glu944Ala
XM_017021975.1:c.2762A>C	XP_016877464.1:p.Glu921Ala
XM_017021976.1:c.2102A>C	XP_016877465.1:p.Glu701Ala
XM_017021978.1:c.1733A>C	XP_016877467.1:p.Glu578Ala
XM_017021979.1:c.1511A>C	XP_016877468.1:p.Glu504Ala
XM_017021980.1:c.1511A>C	XP_016877469.1:p.Glu504Ala
XM_017021982.1:c.1220A>C	XP_016877471.1:p.Glu407Ala
XM_017021983.1:c.1004A>C	XP_016877472.1:p.Glu335Ala
NM_139057.4:c.2549A>C MANE Select	NP_620688.2:p.Glu850Ala