Canonical Allele Identifier: CA393943748

Gene: ADAMTS17

Linked Data

• dbSNP Id: rs767656253
• MyVariant Identifiers: chr15:g.100821436T>G (hg19) ; chr15:g.100281231T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100281231T>G , CM000677.2:g.100281231T>G	GRCh38
NC_000015.9:g.100821436T>G , CM000677.1:g.100821436T>G	GRCh37
NC_000015.8:g.98638959T>G	NCBI36
NG_016287.1:g.65748A>C
NG_016287.2:g.65748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.787A>C MANE Select	ENSP00000268070.4:p.Met263Leu
ENST00000568565.2:c.787A>C	ENSP00000456161.2:p.Met263Leu
ENST00000268070.8:c.787A>C	ENSP00000268070.4:p.Met263Leu
ENST00000378898.8:n.468A>C
ENST00000558960.1:c.*209A>C	ENSP00000453604.1:n.*209A>C
NM_139057.2:c.787A>C	NP_620688.2:p.Met263Leu
XM_005254872.2:c.787A>C	XP_005254929.1:p.Met263Leu
XM_011521312.1:c.787A>C	XP_011519614.1:p.Met263Leu
NM_139057.3:c.787A>C	NP_620688.2:p.Met263Leu
XM_005254872.3:c.787A>C	XP_005254929.1:p.Met263Leu
XM_011521312.2:c.787A>C	XP_011519614.1:p.Met263Leu
XM_017021973.2:c.787A>C	XP_016877462.1:p.Met263Leu
XM_017021974.1:c.787A>C	XP_016877463.1:p.Met263Leu
XM_017021975.1:c.787A>C	XP_016877464.1:p.Met263Leu
XM_017021976.1:c.58A>C	XP_016877465.1:p.Met20Leu
XM_017021977.1:c.787A>C	XP_016877466.1:p.Met263Leu
XM_017021981.1:c.787A>C	XP_016877470.1:p.Met263Leu
XM_017021984.1:c.58A>C	XP_016877473.1:p.Met20Leu
XR_001751118.1:n.1809A>C
XR_001751119.1:n.1809A>C
XR_001751120.1:n.1809A>C
NM_139057.4:c.787A>C MANE Select	NP_620688.2:p.Met263Leu