Canonical Allele Identifier: CA1300570876

Gene: GPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579008_156579009delinsAT , CM000664.2:g.156579008_156579009delinsAT	GRCh38
NC_000002.11:g.157435520_157435521delinsAT , CM000664.1:g.157435520_157435521delinsAT	GRCh37
NC_000002.10:g.157143766_157143767delinsAT	NCBI36
NG_016606.1:g.148556_148557delinsAT
NG_016606.2:g.148556_148557delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1880+7_1880+8delinsAT MANE Select	ENSP00000409708.2:n.1880+7_1880+8delinsAT
ENST00000310454.10:c.1880+7_1880+8delinsAT	ENSP00000308610.5:n.1880+7_1880+8delinsAT
ENST00000409125.8:c.1502+7_1502+8delinsAT	ENSP00000386484.5:n.1502+7_1502+8delinsAT
ENST00000409674.5:c.1880+7_1880+8delinsAT	ENSP00000386425.1:n.1880+7_1880+8delinsAT
ENST00000409861.5:c.1880+7_1880+8delinsAT	ENSP00000386626.1:n.1880+7_1880+8delinsAT
ENST00000438166.6:c.1880+7_1880+8delinsAT	ENSP00000409708.2:n.1880+7_1880+8delinsAT
ENST00000464846.5:n.241_242delinsAT
ENST00000540309.5:c.1135-78_1135-77delinsAT	ENSP00000440892.1:n.1135-78_1135-77delinsAT
NM_000408.4:c.1880+7_1880+8delinsAT	NP_000399.3:n.1880+7_1880+8delinsAT
NM_001083112.2:c.1880+7_1880+8delinsAT	NP_001076581.2:n.1880+7_1880+8delinsAT
XM_005246469.1:c.1880+7_1880+8delinsAT	XP_005246526.1:n.1880+7_1880+8delinsAT
XM_005246470.3:c.1778+7_1778+8delinsAT	XP_005246527.1:n.1778+7_1778+8delinsAT
XM_011510977.1:c.1880+7_1880+8delinsAT	XP_011509279.1:n.1880+7_1880+8delinsAT
XM_011510978.1:c.1778+7_1778+8delinsAT	XP_011509280.1:n.1778+7_1778+8delinsAT
XM_011510979.1:c.1502+7_1502+8delinsAT	XP_011509281.1:n.1502+7_1502+8delinsAT
XM_011510980.1:c.1199+7_1199+8delinsAT	XP_011509282.1:n.1199+7_1199+8delinsAT
XM_005246469.2:c.1880+7_1880+8delinsAT	XP_005246526.1:n.1880+7_1880+8delinsAT
XM_011510977.2:c.1880+7_1880+8delinsAT	XP_011509279.1:n.1880+7_1880+8delinsAT
XM_011510978.2:c.1778+7_1778+8delinsAT	XP_011509280.1:n.1778+7_1778+8delinsAT
XM_017003830.1:c.1880+7_1880+8delinsAT	XP_016859319.1:n.1880+7_1880+8delinsAT
XM_024452798.1:c.1880+7_1880+8delinsAT	XP_024308566.1:n.1880+7_1880+8delinsAT
NM_000408.5:c.1880+7_1880+8delinsAT MANE Select	NP_000399.3:n.1880+7_1880+8delinsAT
NM_001083112.3:c.1880+7_1880+8delinsAT	NP_001076581.2:n.1880+7_1880+8delinsAT