Canonical Allele Identifier: CA672110

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21861754T>A , CM000663.2:g.21861754T>A	GRCh38
NC_000001.10:g.22188247T>A , CM000663.1:g.22188247T>A	GRCh37
NC_000001.9:g.22060834T>A	NCBI36
NG_016740.1:g.80504A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005529.7:c.4955+3A>T MANE Select	NP_005520.4:n.4955+3A>T
ENST00000374695.8:c.4955+3A>T MANE Select	ENSP00000363827.3:n.4955+3A>T
NM_001291860.1:c.4958+3A>T	NP_001278789.1:n.4958+3A>T
NM_001291860.2:c.4958+3A>T	NP_001278789.1:n.4958+3A>T
NM_005529.6:c.4955+3A>T	NP_005520.4:n.4955+3A>T
ENST00000374695.7:c.4955+3A>T	ENSP00000363827.3:n.4955+3A>T
XM_006710594.2:c.5501+3A>T	XP_006710657.1:n.5501+3A>T
XM_006710595.2:c.5453+3A>T	XP_006710658.1:n.5453+3A>T
XM_006710596.2:c.5432+3A>T	XP_006710659.1:n.5432+3A>T
XM_006710597.2:c.4955+3A>T	XP_006710660.1:n.4955+3A>T
XM_011541317.1:c.5504+3A>T	XP_011539619.1:n.5504+3A>T
XM_011541318.1:c.5504+3A>T	XP_011539620.1:n.5504+3A>T
XM_011541318.2:c.5504+3A>T	XP_011539620.1:n.5504+3A>T
XM_011541319.1:c.5504+3A>T	XP_011539621.1:n.5504+3A>T
XM_011541320.1:c.5504+3A>T	XP_011539622.1:n.5504+3A>T
XM_011541321.1:c.5009+3A>T	XP_011539623.1:n.5009+3A>T
XM_011541322.1:c.5504+3A>T	XP_011539624.1:n.5504+3A>T
XM_017001120.1:c.5150+3A>T	XP_016856609.1:n.5150+3A>T
XM_017001121.1:c.5099+3A>T	XP_016856610.1:n.5099+3A>T
XM_017001122.1:c.5096+3A>T	XP_016856611.1:n.5096+3A>T