Canonical Allele Identifier: CA393692372

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589102G>C (hg19) ; chr15:g.100048897G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048897G>C , CM000677.2:g.100048897G>C	GRCh38
NC_000015.9:g.100589102G>C , CM000677.1:g.100589102G>C	GRCh37
NC_000015.8:g.98406625G>C	NCBI36
NG_016287.1:g.298082C>G
NG_016287.2:g.298082C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2551C>G MANE Select	ENSP00000268070.4:p.Pro851Ala
ENST00000568565.2:c.2632C>G	ENSP00000456161.2:p.Pro878Ala
ENST00000268070.8:c.2551C>G	ENSP00000268070.4:p.Pro851Ala
NM_139057.2:c.2551C>G	NP_620688.2:p.Pro851Ala
XM_005254872.2:c.2632C>G	XP_005254929.1:p.Pro878Ala
XM_011521312.1:c.2701C>G	XP_011519614.1:p.Pro901Ala
NM_139057.3:c.2551C>G	NP_620688.2:p.Pro851Ala
XM_005254872.3:c.2632C>G	XP_005254929.1:p.Pro878Ala
XM_011521312.2:c.2701C>G	XP_011519614.1:p.Pro901Ala
XM_017021973.2:c.2833C>G	XP_016877462.1:p.Pro945Ala
XM_017021974.1:c.2833C>G	XP_016877463.1:p.Pro945Ala
XM_017021975.1:c.2764C>G	XP_016877464.1:p.Pro922Ala
XM_017021976.1:c.2104C>G	XP_016877465.1:p.Pro702Ala
XM_017021978.1:c.1735C>G	XP_016877467.1:p.Pro579Ala
XM_017021979.1:c.1513C>G	XP_016877468.1:p.Pro505Ala
XM_017021980.1:c.1513C>G	XP_016877469.1:p.Pro505Ala
XM_017021982.1:c.1222C>G	XP_016877471.1:p.Pro408Ala
XM_017021983.1:c.1006C>G	XP_016877472.1:p.Pro336Ala
NM_139057.4:c.2551C>G MANE Select	NP_620688.2:p.Pro851Ala