Canonical Allele Identifier: CA393692261

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589069G>C (hg19) ; chr15:g.100048864G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048864G>C , CM000677.2:g.100048864G>C	GRCh38
NC_000015.9:g.100589069G>C , CM000677.1:g.100589069G>C	GRCh37
NC_000015.8:g.98406592G>C	NCBI36
NG_016287.1:g.298115C>G
NG_016287.2:g.298115C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2584C>G MANE Select	ENSP00000268070.4:p.Gln862Glu
ENST00000568565.2:c.2665C>G	ENSP00000456161.2:p.Gln889Glu
ENST00000268070.8:c.2584C>G	ENSP00000268070.4:p.Gln862Glu
NM_139057.2:c.2584C>G	NP_620688.2:p.Gln862Glu
XM_005254872.2:c.2665C>G	XP_005254929.1:p.Gln889Glu
XM_011521312.1:c.2734C>G	XP_011519614.1:p.Gln912Glu
NM_139057.3:c.2584C>G	NP_620688.2:p.Gln862Glu
XM_005254872.3:c.2665C>G	XP_005254929.1:p.Gln889Glu
XM_011521312.2:c.2734C>G	XP_011519614.1:p.Gln912Glu
XM_017021973.2:c.2866C>G	XP_016877462.1:p.Gln956Glu
XM_017021974.1:c.2866C>G	XP_016877463.1:p.Gln956Glu
XM_017021975.1:c.2797C>G	XP_016877464.1:p.Gln933Glu
XM_017021976.1:c.2137C>G	XP_016877465.1:p.Gln713Glu
XM_017021978.1:c.1768C>G	XP_016877467.1:p.Gln590Glu
XM_017021979.1:c.1546C>G	XP_016877468.1:p.Gln516Glu
XM_017021980.1:c.1546C>G	XP_016877469.1:p.Gln516Glu
XM_017021982.1:c.1255C>G	XP_016877471.1:p.Gln419Glu
XM_017021983.1:c.1039C>G	XP_016877472.1:p.Gln347Glu
NM_139057.4:c.2584C>G MANE Select	NP_620688.2:p.Gln862Glu