Canonical Allele Identifier: CA492369937

Gene: ADAMTS17

Linked Data

• MyVariant Identifiers: chr15:g.100589106T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100048901T>G , CM000677.2:g.100048901T>G	GRCh38
NC_000015.9:g.100589106T>G , CM000677.1:g.100589106T>G	GRCh37
NC_000015.8:g.98406629T>G	NCBI36
NG_016287.1:g.298078A>C
NG_016287.2:g.298078A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268070.9:c.2547A>C MANE Select	ENSP00000268070.4:p.Pro849=
ENST00000568565.2:c.2628A>C	ENSP00000456161.2:p.Pro876=
ENST00000268070.8:c.2547A>C	ENSP00000268070.4:p.Pro849=
NM_139057.2:c.2547A>C	NP_620688.2:p.Pro849=
XM_005254872.2:c.2628A>C	XP_005254929.1:p.Pro876=
XM_011521312.1:c.2697A>C	XP_011519614.1:p.Pro899=
NM_139057.3:c.2547A>C	NP_620688.2:p.Pro849=
XM_005254872.3:c.2628A>C	XP_005254929.1:p.Pro876=
XM_011521312.2:c.2697A>C	XP_011519614.1:p.Pro899=
XM_017021973.2:c.2829A>C	XP_016877462.1:p.Pro943=
XM_017021974.1:c.2829A>C	XP_016877463.1:p.Pro943=
XM_017021975.1:c.2760A>C	XP_016877464.1:p.Pro920=
XM_017021976.1:c.2100A>C	XP_016877465.1:p.Pro700=
XM_017021978.1:c.1731A>C	XP_016877467.1:p.Pro577=
XM_017021979.1:c.1509A>C	XP_016877468.1:p.Pro503=
XM_017021980.1:c.1509A>C	XP_016877469.1:p.Pro503=
XM_017021982.1:c.1218A>C	XP_016877471.1:p.Pro406=
XM_017021983.1:c.1002A>C	XP_016877472.1:p.Pro334=
NM_139057.4:c.2547A>C MANE Select	NP_620688.2:p.Pro849=