Canonical Allele Identifier: CA670349

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21839543G>A , CM000663.2:g.21839543G>A	GRCh38
NC_000001.10:g.22166036G>A , CM000663.1:g.22166036G>A	GRCh37
NC_000001.9:g.22038623G>A	NCBI36
NG_016740.1:g.102715C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.9717C>T MANE Select	ENSP00000363827.3:p.Pro3239=
ENST00000374695.7:c.9717C>T	ENSP00000363827.3:p.Pro3239=
NM_001291860.1:c.9720C>T	NP_001278789.1:p.Pro3240=
NM_005529.6:c.9717C>T	NP_005520.4:p.Pro3239=
XM_006710594.2:c.10263C>T	XP_006710657.1:p.Pro3421=
XM_006710595.2:c.10215C>T	XP_006710658.1:p.Pro3405=
XM_006710596.2:c.10194C>T	XP_006710659.1:p.Pro3398=
XM_006710597.2:c.9717C>T	XP_006710660.1:p.Pro3239=
XM_011541317.1:c.10266C>T	XP_011539619.1:p.Pro3422=
XM_011541318.1:c.10266C>T	XP_011539620.1:p.Pro3422=
XM_011541319.1:c.10266C>T	XP_011539621.1:p.Pro3422=
XM_011541320.1:c.9987C>T	XP_011539622.1:p.Pro3329=
XM_011541321.1:c.9771C>T	XP_011539623.1:p.Pro3257=
XM_011541318.2:c.10266C>T	XP_011539620.1:p.Pro3422=
XM_017001120.1:c.9912C>T	XP_016856609.1:p.Pro3304=
XM_017001121.1:c.9861C>T	XP_016856610.1:p.Pro3287=
XM_017001122.1:c.9858C>T	XP_016856611.1:p.Pro3286=
NM_005529.7:c.9717C>T MANE Select	NP_005520.4:p.Pro3239=
NM_001291860.2:c.9720C>T	NP_001278789.1:p.Pro3240=