Canonical Allele Identifier: CA416679259

Gene: HSPG2

Linked Data

• MyVariant Identifiers: chr1:g.22168754C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21842261C>A , CM000663.2:g.21842261C>A	GRCh38
NC_000001.10:g.22168754C>A , CM000663.1:g.22168754C>A	GRCh37
NC_000001.9:g.22041341C>A	NCBI36
NG_016740.1:g.99997G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374695.8:c.9030G>T MANE Select	ENSP00000363827.3:p.Pro3010=
ENST00000374695.7:c.9030G>T	ENSP00000363827.3:p.Pro3010=
NM_001291860.1:c.9033G>T	NP_001278789.1:p.Pro3011=
NM_005529.6:c.9030G>T	NP_005520.4:p.Pro3010=
XM_006710594.2:c.9576G>T	XP_006710657.1:p.Pro3192=
XM_006710595.2:c.9528G>T	XP_006710658.1:p.Pro3176=
XM_006710596.2:c.9507G>T	XP_006710659.1:p.Pro3169=
XM_006710597.2:c.9030G>T	XP_006710660.1:p.Pro3010=
XM_011541317.1:c.9579G>T	XP_011539619.1:p.Pro3193=
XM_011541318.1:c.9579G>T	XP_011539620.1:p.Pro3193=
XM_011541319.1:c.9579G>T	XP_011539621.1:p.Pro3193=
XM_011541320.1:c.9300G>T	XP_011539622.1:p.Pro3100=
XM_011541321.1:c.9084G>T	XP_011539623.1:p.Pro3028=
XM_011541318.2:c.9579G>T	XP_011539620.1:p.Pro3193=
XM_017001120.1:c.9225G>T	XP_016856609.1:p.Pro3075=
XM_017001121.1:c.9174G>T	XP_016856610.1:p.Pro3058=
XM_017001122.1:c.9171G>T	XP_016856611.1:p.Pro3057=
NM_005529.7:c.9030G>T MANE Select	NP_005520.4:p.Pro3010=
NM_001291860.2:c.9033G>T	NP_001278789.1:p.Pro3011=