Canonical Allele Identifier: CA338914001

Gene: HSPG2

Linked Data

• MyVariant Identifiers: chr1:g.22167613T>A (hg19) ; chr1:g.21841120T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21841120T>A , CM000663.2:g.21841120T>A	GRCh38
NC_000001.10:g.22167613T>A , CM000663.1:g.22167613T>A	GRCh37
NC_000001.9:g.22040200T>A	NCBI36
NG_016740.1:g.101138A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374695.8:c.9494A>T MANE Select	ENSP00000363827.3:p.Asp3165Val
ENST00000374695.7:c.9494A>T	ENSP00000363827.3:p.Asp3165Val
NM_001291860.1:c.9497A>T	NP_001278789.1:p.Asp3166Val
NM_005529.6:c.9494A>T	NP_005520.4:p.Asp3165Val
XM_006710594.2:c.10040A>T	XP_006710657.1:p.Asp3347Val
XM_006710595.2:c.9992A>T	XP_006710658.1:p.Asp3331Val
XM_006710596.2:c.9971A>T	XP_006710659.1:p.Asp3324Val
XM_006710597.2:c.9494A>T	XP_006710660.1:p.Asp3165Val
XM_011541317.1:c.10043A>T	XP_011539619.1:p.Asp3348Val
XM_011541318.1:c.10043A>T	XP_011539620.1:p.Asp3348Val
XM_011541319.1:c.10043A>T	XP_011539621.1:p.Asp3348Val
XM_011541320.1:c.9764A>T	XP_011539622.1:p.Asp3255Val
XM_011541321.1:c.9548A>T	XP_011539623.1:p.Asp3183Val
XM_011541318.2:c.10043A>T	XP_011539620.1:p.Asp3348Val
XM_017001120.1:c.9689A>T	XP_016856609.1:p.Asp3230Val
XM_017001121.1:c.9638A>T	XP_016856610.1:p.Asp3213Val
XM_017001122.1:c.9635A>T	XP_016856611.1:p.Asp3212Val
NM_005529.7:c.9494A>T MANE Select	NP_005520.4:p.Asp3165Val
NM_001291860.2:c.9497A>T	NP_001278789.1:p.Asp3166Val