Canonical Allele Identifier: CA670489

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21841540G>A , CM000663.2:g.21841540G>A	GRCh38
NC_000001.10:g.22168033G>A , CM000663.1:g.22168033G>A	GRCh37
NC_000001.9:g.22040620G>A	NCBI36
NG_016740.1:g.100718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9327C>T MANE Select	ENSP00000363827.3:p.His3109=
ENST00000374695.7:c.9327C>T	ENSP00000363827.3:p.His3109=
NM_001291860.1:c.9330C>T	NP_001278789.1:p.His3110=
NM_005529.6:c.9327C>T	NP_005520.4:p.His3109=
XM_006710594.2:c.9873C>T	XP_006710657.1:p.His3291=
XM_006710595.2:c.9825C>T	XP_006710658.1:p.His3275=
XM_006710596.2:c.9804C>T	XP_006710659.1:p.His3268=
XM_006710597.2:c.9327C>T	XP_006710660.1:p.His3109=
XM_011541317.1:c.9876C>T	XP_011539619.1:p.His3292=
XM_011541318.1:c.9876C>T	XP_011539620.1:p.His3292=
XM_011541319.1:c.9876C>T	XP_011539621.1:p.His3292=
XM_011541320.1:c.9597C>T	XP_011539622.1:p.His3199=
XM_011541321.1:c.9381C>T	XP_011539623.1:p.His3127=
XM_011541318.2:c.9876C>T	XP_011539620.1:p.His3292=
XM_017001120.1:c.9522C>T	XP_016856609.1:p.His3174=
XM_017001121.1:c.9471C>T	XP_016856610.1:p.His3157=
XM_017001122.1:c.9468C>T	XP_016856611.1:p.His3156=
NM_005529.7:c.9327C>T MANE Select	NP_005520.4:p.His3109=
NM_001291860.2:c.9330C>T	NP_001278789.1:p.His3110=