Canonical Allele Identifier: CA670722

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21844139C>G , CM000663.2:g.21844139C>G	GRCh38
NC_000001.10:g.22170632C>G , CM000663.1:g.22170632C>G	GRCh37
NC_000001.9:g.22043219C>G	NCBI36
NG_016740.1:g.98119G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005529.7:c.8616+9G>C MANE Select	NP_005520.4:n.8616+9G>C
ENST00000374695.8:c.8616+9G>C MANE Select	ENSP00000363827.3:n.8616+9G>C
NM_001291860.1:c.8619+9G>C	NP_001278789.1:n.8619+9G>C
NM_001291860.2:c.8619+9G>C	NP_001278789.1:n.8619+9G>C
NM_005529.6:c.8616+9G>C	NP_005520.4:n.8616+9G>C
ENST00000374695.7:c.8616+9G>C	ENSP00000363827.3:n.8616+9G>C
XM_006710594.2:c.9162+9G>C	XP_006710657.1:n.9162+9G>C
XM_006710595.2:c.9114+9G>C	XP_006710658.1:n.9114+9G>C
XM_006710596.2:c.9093+9G>C	XP_006710659.1:n.9093+9G>C
XM_006710597.2:c.8616+9G>C	XP_006710660.1:n.8616+9G>C
XM_011541317.1:c.9165+9G>C	XP_011539619.1:n.9165+9G>C
XM_011541318.1:c.9165+9G>C	XP_011539620.1:n.9165+9G>C
XM_011541318.2:c.9165+9G>C	XP_011539620.1:n.9165+9G>C
XM_011541319.1:c.9165+9G>C	XP_011539621.1:n.9165+9G>C
XM_011541320.1:c.8886+9G>C	XP_011539622.1:n.8886+9G>C
XM_011541321.1:c.8670+9G>C	XP_011539623.1:n.8670+9G>C
XM_017001120.1:c.8811+9G>C	XP_016856609.1:n.8811+9G>C
XM_017001121.1:c.8760+9G>C	XP_016856610.1:n.8760+9G>C
XM_017001122.1:c.8757+9G>C	XP_016856611.1:n.8757+9G>C