Canonical Allele Identifier: CA671071

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21848101A>G , CM000663.2:g.21848101A>G	GRCh38
NC_000001.10:g.22174594A>G , CM000663.1:g.22174594A>G	GRCh37
NC_000001.9:g.22047181A>G	NCBI36
NG_016740.1:g.94157T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.7738-8T>C MANE Select	ENSP00000363827.3:n.7738-8T>C
ENST00000374695.7:c.7738-8T>C	ENSP00000363827.3:n.7738-8T>C
NM_001291860.1:c.7741-8T>C	NP_001278789.1:n.7741-8T>C
NM_005529.6:c.7738-8T>C	NP_005520.4:n.7738-8T>C
XM_006710594.2:c.8284-8T>C	XP_006710657.1:n.8284-8T>C
XM_006710595.2:c.8236-8T>C	XP_006710658.1:n.8236-8T>C
XM_006710596.2:c.8215-8T>C	XP_006710659.1:n.8215-8T>C
XM_006710597.2:c.7738-8T>C	XP_006710660.1:n.7738-8T>C
XM_011541317.1:c.8287-8T>C	XP_011539619.1:n.8287-8T>C
XM_011541318.1:c.8287-8T>C	XP_011539620.1:n.8287-8T>C
XM_011541319.1:c.8287-8T>C	XP_011539621.1:n.8287-8T>C
XM_011541320.1:c.8008-8T>C	XP_011539622.1:n.8008-8T>C
XM_011541321.1:c.7792-8T>C	XP_011539623.1:n.7792-8T>C
XM_011541318.2:c.8287-8T>C	XP_011539620.1:n.8287-8T>C
XM_017001120.1:c.7933-8T>C	XP_016856609.1:n.7933-8T>C
XM_017001121.1:c.7882-8T>C	XP_016856610.1:n.7882-8T>C
XM_017001122.1:c.7879-8T>C	XP_016856611.1:n.7879-8T>C
NM_005529.7:c.7738-8T>C MANE Select	NP_005520.4:n.7738-8T>C
NM_001291860.2:c.7741-8T>C	NP_001278789.1:n.7741-8T>C