Canonical Allele Identifier: CA670318

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21839408A>G , CM000663.2:g.21839408A>G	GRCh38
NC_000001.10:g.22165901A>G , CM000663.1:g.22165901A>G	GRCh37
NC_000001.9:g.22038488A>G	NCBI36
NG_016740.1:g.102850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9852T>C MANE Select	ENSP00000363827.3:p.Ala3284=
ENST00000374695.7:c.9852T>C	ENSP00000363827.3:p.Ala3284=
NM_001291860.1:c.9855T>C	NP_001278789.1:p.Ala3285=
NM_005529.6:c.9852T>C	NP_005520.4:p.Ala3284=
XM_006710594.2:c.10398T>C	XP_006710657.1:p.Ala3466=
XM_006710595.2:c.10350T>C	XP_006710658.1:p.Ala3450=
XM_006710596.2:c.10329T>C	XP_006710659.1:p.Ala3443=
XM_006710597.2:c.9852T>C	XP_006710660.1:p.Ala3284=
XM_011541317.1:c.10401T>C	XP_011539619.1:p.Ala3467=
XM_011541318.1:c.10401T>C	XP_011539620.1:p.Ala3467=
XM_011541319.1:c.10401T>C	XP_011539621.1:p.Ala3467=
XM_011541320.1:c.10122T>C	XP_011539622.1:p.Ala3374=
XM_011541321.1:c.9906T>C	XP_011539623.1:p.Ala3302=
XM_011541318.2:c.10401T>C	XP_011539620.1:p.Ala3467=
XM_017001120.1:c.10047T>C	XP_016856609.1:p.Ala3349=
XM_017001121.1:c.9996T>C	XP_016856610.1:p.Ala3332=
XM_017001122.1:c.9993T>C	XP_016856611.1:p.Ala3331=
NM_005529.7:c.9852T>C MANE Select	NP_005520.4:p.Ala3284=
NM_001291860.2:c.9855T>C	NP_001278789.1:p.Ala3285=