Canonical Allele Identifier: CA7757388

Gene: ADAMTS17

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.99974383C>T , CM000677.2:g.99974383C>T	GRCh38
NC_000015.9:g.100514588C>T , CM000677.1:g.100514588C>T	GRCh37
NC_000015.8:g.98332111C>T	NCBI36
NG_016287.1:g.372596G>A
NG_016287.2:g.372596G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.*19G>A MANE Select	ENSP00000268070.4:n.*19G>A
ENST00000268070.8:c.*19G>A	ENSP00000268070.4:n.*19G>A
ENST00000557896.1:n.415G>A
NM_139057.2:c.*19G>A	NP_620688.2:n.*19G>A
XM_005254872.2:c.*19G>A	XP_005254929.1:n.*19G>A
XM_011521312.1:c.*19G>A	XP_011519614.1:n.*19G>A
NM_139057.3:c.*19G>A	NP_620688.2:n.*19G>A
XM_005254872.3:c.*19G>A	XP_005254929.1:n.*19G>A
XM_011521312.2:c.*19G>A	XP_011519614.1:n.*19G>A
XM_017021973.2:c.*19G>A	XP_016877462.1:n.*19G>A
XM_017021975.1:c.*19G>A	XP_016877464.1:n.*19G>A
XM_017021976.1:c.*19G>A	XP_016877465.1:n.*19G>A
XM_017021978.1:c.*19G>A	XP_016877467.1:n.*19G>A
XM_017021979.1:c.*19G>A	XP_016877468.1:n.*19G>A
XM_017021980.1:c.*19G>A	XP_016877469.1:n.*19G>A
XM_017021982.1:c.*19G>A	XP_016877471.1:n.*19G>A
XM_017021983.1:c.*19G>A	XP_016877472.1:n.*19G>A
NM_139057.4:c.*19G>A MANE Select	NP_620688.2:n.*19G>A