Canonical Allele Identifier: CA393692317

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589087A>C (hg19) ; chr15:g.100048882A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048882A>C , CM000677.2:g.100048882A>C	GRCh38
NC_000015.9:g.100589087A>C , CM000677.1:g.100589087A>C	GRCh37
NC_000015.8:g.98406610A>C	NCBI36
NG_016287.1:g.298097T>G
NG_016287.2:g.298097T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2566T>G MANE Select	ENSP00000268070.4:p.Cys856Gly
ENST00000568565.2:c.2647T>G	ENSP00000456161.2:p.Cys883Gly
ENST00000268070.8:c.2566T>G	ENSP00000268070.4:p.Cys856Gly
NM_139057.2:c.2566T>G	NP_620688.2:p.Cys856Gly
XM_005254872.2:c.2647T>G	XP_005254929.1:p.Cys883Gly
XM_011521312.1:c.2716T>G	XP_011519614.1:p.Cys906Gly
NM_139057.3:c.2566T>G	NP_620688.2:p.Cys856Gly
XM_005254872.3:c.2647T>G	XP_005254929.1:p.Cys883Gly
XM_011521312.2:c.2716T>G	XP_011519614.1:p.Cys906Gly
XM_017021973.2:c.2848T>G	XP_016877462.1:p.Cys950Gly
XM_017021974.1:c.2848T>G	XP_016877463.1:p.Cys950Gly
XM_017021975.1:c.2779T>G	XP_016877464.1:p.Cys927Gly
XM_017021976.1:c.2119T>G	XP_016877465.1:p.Cys707Gly
XM_017021978.1:c.1750T>G	XP_016877467.1:p.Cys584Gly
XM_017021979.1:c.1528T>G	XP_016877468.1:p.Cys510Gly
XM_017021980.1:c.1528T>G	XP_016877469.1:p.Cys510Gly
XM_017021982.1:c.1237T>G	XP_016877471.1:p.Cys413Gly
XM_017021983.1:c.1021T>G	XP_016877472.1:p.Cys341Gly
NM_139057.4:c.2566T>G MANE Select	NP_620688.2:p.Cys856Gly