Canonical Allele Identifier: CA2752803536

Gene: GPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579211_156579212insCCAAACACACCCAACAC , CM000664.2:g.156579211_156579212insCCAAACACACCCAACAC	GRCh38
NC_000002.11:g.157435723_157435724insCCAAACACACCCAACAC , CM000664.1:g.157435723_157435724insCCAAACACACCCAACAC	GRCh37
NC_000002.10:g.157143969_157143970insCCAAACACACCCAACAC	NCBI36
NG_016606.1:g.148759_148760insCCAAACACACCCAACAC
NG_016606.2:g.148759_148760insCCAAACACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1959+47_1959+48insCCAAACACACCCAACAC MANE Select	ENSP00000409708.2:n.1959+47_1959+48insCCAAACACACCCAACAC
ENST00000310454.10:c.1959+47_1959+48insCCAAACACACCCAACAC	ENSP00000308610.5:n.1959+47_1959+48insCCAAACACACCCAACAC
ENST00000409125.8:c.1581+47_1581+48insCCAAACACACCCAACAC	ENSP00000386484.5:n.1581+47_1581+48insCCAAACACACCCAACAC
ENST00000409674.5:c.1959+47_1959+48insCCAAACACACCCAACAC	ENSP00000386425.1:n.1959+47_1959+48insCCAAACACACCCAACAC
ENST00000409861.5:c.1959+47_1959+48insCCAAACACACCCAACAC	ENSP00000386626.1:n.1959+47_1959+48insCCAAACACACCCAACAC
ENST00000438166.6:c.1959+47_1959+48insCCAAACACACCCAACAC	ENSP00000409708.2:n.1959+47_1959+48insCCAAACACACCCAACAC
ENST00000464846.5:n.397+47_397+48insCCAAACACACCCAACAC
ENST00000492005.1:n.82+47_82+48insCCAAACACACCCAACAC
ENST00000540309.5:c.*73+47_*73+48insCCAAACACACCCAACAC	ENSP00000440892.1:n.*73+47_*73+48insCCAAACACACCCAACAC
NM_000408.4:c.1959+47_1959+48insCCAAACACACCCAACAC	NP_000399.3:n.1959+47_1959+48insCCAAACACACCCAACAC
NM_001083112.2:c.1959+47_1959+48insCCAAACACACCCAACAC	NP_001076581.2:n.1959+47_1959+48insCCAAACACACCCAACAC
XM_005246469.1:c.1959+47_1959+48insCCAAACACACCCAACAC	XP_005246526.1:n.1959+47_1959+48insCCAAACACACCCAACAC
XM_005246470.3:c.1857+47_1857+48insCCAAACACACCCAACAC	XP_005246527.1:n.1857+47_1857+48insCCAAACACACCCAACAC
XM_011510977.1:c.1959+47_1959+48insCCAAACACACCCAACAC	XP_011509279.1:n.1959+47_1959+48insCCAAACACACCCAACAC
XM_011510978.1:c.1857+47_1857+48insCCAAACACACCCAACAC	XP_011509280.1:n.1857+47_1857+48insCCAAACACACCCAACAC
XM_011510979.1:c.1581+47_1581+48insCCAAACACACCCAACAC	XP_011509281.1:n.1581+47_1581+48insCCAAACACACCCAACAC
XM_011510980.1:c.1278+47_1278+48insCCAAACACACCCAACAC	XP_011509282.1:n.1278+47_1278+48insCCAAACACACCCAACAC
XM_005246469.2:c.1959+47_1959+48insCCAAACACACCCAACAC	XP_005246526.1:n.1959+47_1959+48insCCAAACACACCCAACAC
XM_011510977.2:c.1959+47_1959+48insCCAAACACACCCAACAC	XP_011509279.1:n.1959+47_1959+48insCCAAACACACCCAACAC
XM_011510978.2:c.1857+47_1857+48insCCAAACACACCCAACAC	XP_011509280.1:n.1857+47_1857+48insCCAAACACACCCAACAC
XM_017003830.1:c.1959+47_1959+48insCCAAACACACCCAACAC	XP_016859319.1:n.1959+47_1959+48insCCAAACACACCCAACAC
XM_024452798.1:c.1959+47_1959+48insCCAAACACACCCAACAC	XP_024308566.1:n.1959+47_1959+48insCCAAACACACCCAACAC
NM_000408.5:c.1959+47_1959+48insCCAAACACACCCAACAC MANE Select	NP_000399.3:n.1959+47_1959+48insCCAAACACACCCAACAC
NM_001083112.3:c.1959+47_1959+48insCCAAACACACCCAACAC	NP_001076581.2:n.1959+47_1959+48insCCAAACACACCCAACAC