Canonical Allele Identifier: CA1300570937

Gene: GPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579122_156579123delinsGA , CM000664.2:g.156579122_156579123delinsGA	GRCh38
NC_000002.11:g.157435634_157435635delinsGA , CM000664.1:g.157435634_157435635delinsGA	GRCh37
NC_000002.10:g.157143880_157143881delinsGA	NCBI36
NG_016606.1:g.148670_148671delinsGA
NG_016606.2:g.148670_148671delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1917_1918delinsGA MANE Select	ENSP00000409708.2:p.Gln639=
ENST00000310454.10:c.1917_1918delinsGA	ENSP00000308610.5:p.Gln639=
ENST00000409125.8:c.1539_1540delinsGA	ENSP00000386484.5:p.Gln513=
ENST00000409674.5:c.1917_1918delinsGA	ENSP00000386425.1:p.Gln639=
ENST00000409861.5:c.1917_1918delinsGA	ENSP00000386626.1:p.Gln639=
ENST00000438166.6:c.1917_1918delinsGA	ENSP00000409708.2:p.Gln639=
ENST00000464846.5:n.355_356delinsGA
ENST00000492005.1:n.40_41delinsGA
ENST00000540309.5:c.*31_*32delinsGA	ENSP00000440892.1:n.*31_*32delinsGA
NM_000408.4:c.1917_1918delinsGA	NP_000399.3:p.Gln639=
NM_001083112.2:c.1917_1918delinsGA	NP_001076581.2:p.Gln639=
XM_005246469.1:c.1917_1918delinsGA	XP_005246526.1:p.Gln639=
XM_005246470.3:c.1815_1816delinsGA	XP_005246527.1:p.Gln605=
XM_011510977.1:c.1917_1918delinsGA	XP_011509279.1:p.Gln639=
XM_011510978.1:c.1815_1816delinsGA	XP_011509280.1:p.Gln605=
XM_011510979.1:c.1539_1540delinsGA	XP_011509281.1:p.Gln513=
XM_011510980.1:c.1236_1237delinsGA	XP_011509282.1:p.Gln412=
XM_005246469.2:c.1917_1918delinsGA	XP_005246526.1:p.Gln639=
XM_011510977.2:c.1917_1918delinsGA	XP_011509279.1:p.Gln639=
XM_011510978.2:c.1815_1816delinsGA	XP_011509280.1:p.Gln605=
XM_017003830.1:c.1917_1918delinsGA	XP_016859319.1:p.Gln639=
XM_024452798.1:c.1917_1918delinsGA	XP_024308566.1:p.Gln639=
NM_000408.5:c.1917_1918delinsGA MANE Select	NP_000399.3:p.Gln639=
NM_001083112.3:c.1917_1918delinsGA	NP_001076581.2:p.Gln639=