Canonical Allele Identifier: CA338909093

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21834790C>G , CM000663.2:g.21834790C>G	GRCh38
NC_000001.10:g.22161283C>G , CM000663.1:g.22161283C>G	GRCh37
NC_000001.9:g.22033870C>G	NCBI36
NG_016740.1:g.107468G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.10609G>C MANE Select	ENSP00000363827.3:p.Gly3537Arg
ENST00000374695.7:c.10609G>C	ENSP00000363827.3:p.Gly3537Arg
ENST00000471322.2:n.964G>C
NM_001291860.1:c.10612G>C	NP_001278789.1:p.Gly3538Arg
NM_005529.6:c.10609G>C	NP_005520.4:p.Gly3537Arg
XM_006710594.2:c.11155G>C	XP_006710657.1:p.Gly3719Arg
XM_006710595.2:c.11107G>C	XP_006710658.1:p.Gly3703Arg
XM_006710596.2:c.11086G>C	XP_006710659.1:p.Gly3696Arg
XM_006710597.2:c.10609G>C	XP_006710660.1:p.Gly3537Arg
XM_011541317.1:c.11158G>C	XP_011539619.1:p.Gly3720Arg
XM_011541318.1:c.11158G>C	XP_011539620.1:p.Gly3720Arg
XM_011541319.1:c.11158G>C	XP_011539621.1:p.Gly3720Arg
XM_011541320.1:c.10879G>C	XP_011539622.1:p.Gly3627Arg
XM_011541321.1:c.10663G>C	XP_011539623.1:p.Gly3555Arg
XM_011541318.2:c.11158G>C	XP_011539620.1:p.Gly3720Arg
XM_017001120.1:c.10804G>C	XP_016856609.1:p.Gly3602Arg
XM_017001121.1:c.10753G>C	XP_016856610.1:p.Gly3585Arg
XM_017001122.1:c.10750G>C	XP_016856611.1:p.Gly3584Arg
NM_005529.7:c.10609G>C MANE Select	NP_005520.4:p.Gly3537Arg
NM_001291860.2:c.10612G>C	NP_001278789.1:p.Gly3538Arg