Canonical Allele Identifier: CA2630606037

Gene: ADAMTS17

Linked Data

• gnomAD v4: 15-100048793-C-CGT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048793_100048794insGT , CM000677.2:g.100048793_100048794insGT	GRCh38
NC_000015.9:g.100588998_100588999insGT , CM000677.1:g.100588998_100588999insGT	GRCh37
NC_000015.8:g.98406521_98406522insGT	NCBI36
NG_016287.1:g.298185_298186insAC
NG_016287.2:g.298185_298186insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2591+63_2591+64insAC MANE Select	ENSP00000268070.4:n.2591+63_2591+64insAC
ENST00000568565.2:c.2672+63_2672+64insAC	ENSP00000456161.2:n.2672+63_2672+64insAC
ENST00000268070.8:c.2591+63_2591+64insAC	ENSP00000268070.4:n.2591+63_2591+64insAC
NM_139057.2:c.2591+63_2591+64insAC	NP_620688.2:n.2591+63_2591+64insAC
XM_005254872.2:c.2672+63_2672+64insAC	XP_005254929.1:n.2672+63_2672+64insAC
XM_011521312.1:c.2741+63_2741+64insAC	XP_011519614.1:n.2741+63_2741+64insAC
NM_139057.3:c.2591+63_2591+64insAC	NP_620688.2:n.2591+63_2591+64insAC
XM_005254872.3:c.2672+63_2672+64insAC	XP_005254929.1:n.2672+63_2672+64insAC
XM_011521312.2:c.2741+63_2741+64insAC	XP_011519614.1:n.2741+63_2741+64insAC
XM_017021973.2:c.2873+63_2873+64insAC	XP_016877462.1:n.2873+63_2873+64insAC
XM_017021974.1:c.2873+63_2873+64insAC	XP_016877463.1:n.2873+63_2873+64insAC
XM_017021975.1:c.2804+63_2804+64insAC	XP_016877464.1:n.2804+63_2804+64insAC
XM_017021976.1:c.2144+63_2144+64insAC	XP_016877465.1:n.2144+63_2144+64insAC
XM_017021978.1:c.1775+63_1775+64insAC	XP_016877467.1:n.1775+63_1775+64insAC
XM_017021979.1:c.1553+63_1553+64insAC	XP_016877468.1:n.1553+63_1553+64insAC
XM_017021980.1:c.1553+63_1553+64insAC	XP_016877469.1:n.1553+63_1553+64insAC
XM_017021982.1:c.1262+63_1262+64insAC	XP_016877471.1:n.1262+63_1262+64insAC
XM_017021983.1:c.1046+63_1046+64insAC	XP_016877472.1:n.1046+63_1046+64insAC
NM_139057.4:c.2591+63_2591+64insAC MANE Select	NP_620688.2:n.2591+63_2591+64insAC