Canonical Allele Identifier: CA717853013

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs1429904038
• gnomAD v3: 15-99973200-C-G
• gnomAD v4: 15-99973200-C-G
• MyVariant Identifiers: chr15:g.100513405C>G (hg19) ; chr15:g.99973200C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.99973200C>G , CM000677.2:g.99973200C>G	GRCh38
NC_000015.9:g.100513405C>G , CM000677.1:g.100513405C>G	GRCh37
NC_000015.8:g.98330928C>G	NCBI36
NG_016287.1:g.373779G>C
NG_016287.2:g.373779G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.*1202G>C MANE Select	ENSP00000268070.4:n.*1202G>C
ENST00000268070.8:c.*1202G>C	ENSP00000268070.4:n.*1202G>C
ENST00000557896.1:n.1501G>C
NM_139057.2:c.*1202G>C	NP_620688.2:n.*1202G>C
XM_005254872.2:c.*1202G>C	XP_005254929.1:n.*1202G>C
XM_011521312.1:c.*1202G>C	XP_011519614.1:n.*1202G>C
XR_429624.2:n.1744-426C>G
NM_139057.3:c.*1202G>C	NP_620688.2:n.*1202G>C
XM_005254872.3:c.*1202G>C	XP_005254929.1:n.*1202G>C
XM_011521312.2:c.*1202G>C	XP_011519614.1:n.*1202G>C
XM_017021973.2:c.*1202G>C	XP_016877462.1:n.*1202G>C
XM_017021975.1:c.*1202G>C	XP_016877464.1:n.*1202G>C
XM_017021976.1:c.*1202G>C	XP_016877465.1:n.*1202G>C
XM_017021978.1:c.*1202G>C	XP_016877467.1:n.*1202G>C
XM_017021979.1:c.*1202G>C	XP_016877468.1:n.*1202G>C
XM_017021980.1:c.*1202G>C	XP_016877469.1:n.*1202G>C
XM_017021982.1:c.*1202G>C	XP_016877471.1:n.*1202G>C
XM_017021983.1:c.*1202G>C	XP_016877472.1:n.*1202G>C
NM_139057.4:c.*1202G>C MANE Select	NP_620688.2:n.*1202G>C