Canonical Allele Identifier: CA620083793

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs1164910966
• gnomAD v2: 15-100589226-G-C
• gnomAD v4: 15-100049021-G-C
• MyVariant Identifiers: chr15:g.100589226G>C (hg19) ; chr15:g.100049021G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100049021G>C , CM000677.2:g.100049021G>C	GRCh38
NC_000015.9:g.100589226G>C , CM000677.1:g.100589226G>C	GRCh37
NC_000015.8:g.98406749G>C	NCBI36
NG_016287.1:g.297958C>G
NG_016287.2:g.297958C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2456-29C>G MANE Select	ENSP00000268070.4:n.2456-29C>G
ENST00000568565.2:c.2537-29C>G	ENSP00000456161.2:n.2537-29C>G
ENST00000268070.8:c.2456-29C>G	ENSP00000268070.4:n.2456-29C>G
NM_139057.2:c.2456-29C>G	NP_620688.2:n.2456-29C>G
XM_005254872.2:c.2537-29C>G	XP_005254929.1:n.2537-29C>G
XM_011521312.1:c.2606-29C>G	XP_011519614.1:n.2606-29C>G
NM_139057.3:c.2456-29C>G	NP_620688.2:n.2456-29C>G
XM_005254872.3:c.2537-29C>G	XP_005254929.1:n.2537-29C>G
XM_011521312.2:c.2606-29C>G	XP_011519614.1:n.2606-29C>G
XM_017021973.2:c.2738-29C>G	XP_016877462.1:n.2738-29C>G
XM_017021974.1:c.2738-29C>G	XP_016877463.1:n.2738-29C>G
XM_017021975.1:c.2669-29C>G	XP_016877464.1:n.2669-29C>G
XM_017021976.1:c.2009-29C>G	XP_016877465.1:n.2009-29C>G
XM_017021978.1:c.1640-29C>G	XP_016877467.1:n.1640-29C>G
XM_017021979.1:c.1418-29C>G	XP_016877468.1:n.1418-29C>G
XM_017021980.1:c.1418-29C>G	XP_016877469.1:n.1418-29C>G
XM_017021982.1:c.1127-29C>G	XP_016877471.1:n.1127-29C>G
XM_017021983.1:c.911-29C>G	XP_016877472.1:n.911-29C>G
NM_139057.4:c.2456-29C>G MANE Select	NP_620688.2:n.2456-29C>G