Canonical Allele Identifier: CA393692403

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589108G>T (hg19) ; chr15:g.100048903G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048903G>T , CM000677.2:g.100048903G>T	GRCh38
NC_000015.9:g.100589108G>T , CM000677.1:g.100589108G>T	GRCh37
NC_000015.8:g.98406631G>T	NCBI36
NG_016287.1:g.298076C>A
NG_016287.2:g.298076C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2545C>A MANE Select	ENSP00000268070.4:p.Pro849Thr
ENST00000568565.2:c.2626C>A	ENSP00000456161.2:p.Pro876Thr
ENST00000268070.8:c.2545C>A	ENSP00000268070.4:p.Pro849Thr
NM_139057.2:c.2545C>A	NP_620688.2:p.Pro849Thr
XM_005254872.2:c.2626C>A	XP_005254929.1:p.Pro876Thr
XM_011521312.1:c.2695C>A	XP_011519614.1:p.Pro899Thr
NM_139057.3:c.2545C>A	NP_620688.2:p.Pro849Thr
XM_005254872.3:c.2626C>A	XP_005254929.1:p.Pro876Thr
XM_011521312.2:c.2695C>A	XP_011519614.1:p.Pro899Thr
XM_017021973.2:c.2827C>A	XP_016877462.1:p.Pro943Thr
XM_017021974.1:c.2827C>A	XP_016877463.1:p.Pro943Thr
XM_017021975.1:c.2758C>A	XP_016877464.1:p.Pro920Thr
XM_017021976.1:c.2098C>A	XP_016877465.1:p.Pro700Thr
XM_017021978.1:c.1729C>A	XP_016877467.1:p.Pro577Thr
XM_017021979.1:c.1507C>A	XP_016877468.1:p.Pro503Thr
XM_017021980.1:c.1507C>A	XP_016877469.1:p.Pro503Thr
XM_017021982.1:c.1216C>A	XP_016877471.1:p.Pro406Thr
XM_017021983.1:c.1000C>A	XP_016877472.1:p.Pro334Thr
NM_139057.4:c.2545C>A MANE Select	NP_620688.2:p.Pro849Thr