Canonical Allele Identifier: CA275472820

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs781434694
• gnomAD v2: 15-100588896-A-G
• gnomAD v3: 15-100048691-A-G
• gnomAD v4: 15-100048691-A-G
• MyVariant Identifiers: chr15:g.100588896A>G (hg19) ; chr15:g.100048691A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048691A>G , CM000677.2:g.100048691A>G	GRCh38
NC_000015.9:g.100588896A>G , CM000677.1:g.100588896A>G	GRCh37
NC_000015.8:g.98406419A>G	NCBI36
NG_016287.1:g.298288T>C
NG_016287.2:g.298288T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+166T>C MANE Select	ENSP00000268070.4:n.2591+166T>C
ENST00000568565.2:c.2672+166T>C	ENSP00000456161.2:n.2672+166T>C
ENST00000268070.8:c.2591+166T>C	ENSP00000268070.4:n.2591+166T>C
NM_139057.2:c.2591+166T>C	NP_620688.2:n.2591+166T>C
XM_005254872.2:c.2672+166T>C	XP_005254929.1:n.2672+166T>C
XM_011521312.1:c.2741+166T>C	XP_011519614.1:n.2741+166T>C
NM_139057.3:c.2591+166T>C	NP_620688.2:n.2591+166T>C
XM_005254872.3:c.2672+166T>C	XP_005254929.1:n.2672+166T>C
XM_011521312.2:c.2741+166T>C	XP_011519614.1:n.2741+166T>C
XM_017021973.2:c.2873+166T>C	XP_016877462.1:n.2873+166T>C
XM_017021974.1:c.2873+166T>C	XP_016877463.1:n.2873+166T>C
XM_017021975.1:c.2804+166T>C	XP_016877464.1:n.2804+166T>C
XM_017021976.1:c.2144+166T>C	XP_016877465.1:n.2144+166T>C
XM_017021978.1:c.1775+166T>C	XP_016877467.1:n.1775+166T>C
XM_017021979.1:c.1553+166T>C	XP_016877468.1:n.1553+166T>C
XM_017021980.1:c.1553+166T>C	XP_016877469.1:n.1553+166T>C
XM_017021982.1:c.1262+166T>C	XP_016877471.1:n.1262+166T>C
XM_017021983.1:c.1046+166T>C	XP_016877472.1:n.1046+166T>C
NM_139057.4:c.2591+166T>C MANE Select	NP_620688.2:n.2591+166T>C