Canonical Allele Identifier: CA275484072

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs537584407
• gnomAD v3: 15-99973046-T-C
• gnomAD v4: 15-99973046-T-C
• MyVariant Identifiers: chr15:g.100513251T>C (hg19) ; chr15:g.99973046T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.99973046T>C , CM000677.2:g.99973046T>C	GRCh38
NC_000015.9:g.100513251T>C , CM000677.1:g.100513251T>C	GRCh37
NC_000015.8:g.98330774T>C	NCBI36
NG_016287.1:g.373933A>G
NG_016287.2:g.373933A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.*1356A>G MANE Select	ENSP00000268070.4:n.*1356A>G
ENST00000268070.8:c.*1356A>G	ENSP00000268070.4:n.*1356A>G
ENST00000557896.1:n.1655A>G
NM_139057.2:c.*1356A>G	NP_620688.2:n.*1356A>G
XM_005254872.2:c.*1356A>G	XP_005254929.1:n.*1356A>G
XM_011521312.1:c.*1356A>G	XP_011519614.1:n.*1356A>G
XR_429624.2:n.1743+313T>C
NM_139057.3:c.*1356A>G	NP_620688.2:n.*1356A>G
XM_005254872.3:c.*1356A>G	XP_005254929.1:n.*1356A>G
XM_011521312.2:c.*1356A>G	XP_011519614.1:n.*1356A>G
XM_017021973.2:c.*1356A>G	XP_016877462.1:n.*1356A>G
XM_017021975.1:c.*1356A>G	XP_016877464.1:n.*1356A>G
XM_017021976.1:c.*1356A>G	XP_016877465.1:n.*1356A>G
XM_017021978.1:c.*1356A>G	XP_016877467.1:n.*1356A>G
XM_017021979.1:c.*1356A>G	XP_016877468.1:n.*1356A>G
XM_017021980.1:c.*1356A>G	XP_016877469.1:n.*1356A>G
XM_017021982.1:c.*1356A>G	XP_016877471.1:n.*1356A>G
XM_017021983.1:c.*1356A>G	XP_016877472.1:n.*1356A>G
NM_139057.4:c.*1356A>G MANE Select	NP_620688.2:n.*1356A>G