Canonical Allele Identifier: CA7758034

Gene: ADAMTS17

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100116867A>G , CM000677.2:g.100116867A>G	GRCh38
NC_000015.9:g.100657072A>G , CM000677.1:g.100657072A>G	GRCh37
NC_000015.8:g.98474595A>G	NCBI36
NG_016287.1:g.230112T>C
NG_016287.2:g.230112T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.1868T>C MANE Select	ENSP00000268070.4:p.Leu623Pro
ENST00000568565.2:c.1868T>C	ENSP00000456161.2:p.Leu623Pro
ENST00000268070.8:c.1868T>C	ENSP00000268070.4:p.Leu623Pro
ENST00000378898.8:n.1549T>C
NM_139057.2:c.1868T>C	NP_620688.2:p.Leu623Pro
XM_005254872.2:c.1868T>C	XP_005254929.1:p.Leu623Pro
XM_011521312.1:c.1868T>C	XP_011519614.1:p.Leu623Pro
NM_139057.3:c.1868T>C	NP_620688.2:p.Leu623Pro
XM_005254872.3:c.1868T>C	XP_005254929.1:p.Leu623Pro
XM_011521312.2:c.1868T>C	XP_011519614.1:p.Leu623Pro
XM_017021973.2:c.2000T>C	XP_016877462.1:p.Leu667Pro
XM_017021974.1:c.2000T>C	XP_016877463.1:p.Leu667Pro
XM_017021975.1:c.2000T>C	XP_016877464.1:p.Leu667Pro
XM_017021976.1:c.1271T>C	XP_016877465.1:p.Leu424Pro
XM_017021977.1:c.2000T>C	XP_016877466.1:p.Leu667Pro
XM_017021978.1:c.902T>C	XP_016877467.1:p.Leu301Pro
XM_017021979.1:c.680T>C	XP_016877468.1:p.Leu227Pro
XM_017021980.1:c.680T>C	XP_016877469.1:p.Leu227Pro
XM_017021981.1:c.2000T>C	XP_016877470.1:p.Leu667Pro
XM_017021982.1:c.389T>C	XP_016877471.1:p.Leu130Pro
XM_017021983.1:c.173T>C	XP_016877472.1:p.Leu58Pro
XM_017021984.1:c.1139T>C	XP_016877473.1:p.Leu380Pro
XR_001751118.1:n.3022T>C
XR_001751119.1:n.3022T>C
XR_001751120.1:n.3022T>C
NM_139057.4:c.1868T>C MANE Select	NP_620688.2:p.Leu623Pro