Canonical Allele Identifier: CA2661544784

Gene: GPD2

Linked Data

• gnomAD v4: 2-156579223-G-GAGAAAAACATCTAATA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579223_156579224insAGAAAAACATCTAATA , CM000664.2:g.156579223_156579224insAGAAAAACATCTAATA	GRCh38
NC_000002.11:g.157435735_157435736insAGAAAAACATCTAATA , CM000664.1:g.157435735_157435736insAGAAAAACATCTAATA	GRCh37
NC_000002.10:g.157143981_157143982insAGAAAAACATCTAATA	NCBI36
NG_016606.1:g.148771_148772insAGAAAAACATCTAATA
NG_016606.2:g.148771_148772insAGAAAAACATCTAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1959+59_1959+60insAGAAAAACATCTAATA MANE Select	ENSP00000409708.2:n.1959+59_1959+60insAGAAAAACATCTAATA
ENST00000310454.10:c.1959+59_1959+60insAGAAAAACATCTAATA	ENSP00000308610.5:n.1959+59_1959+60insAGAAAAACATCTAATA
ENST00000409125.8:c.1581+59_1581+60insAGAAAAACATCTAATA	ENSP00000386484.5:n.1581+59_1581+60insAGAAAAACATCTAATA
ENST00000409674.5:c.1959+59_1959+60insAGAAAAACATCTAATA	ENSP00000386425.1:n.1959+59_1959+60insAGAAAAACATCTAATA
ENST00000409861.5:c.1959+59_1959+60insAGAAAAACATCTAATA	ENSP00000386626.1:n.1959+59_1959+60insAGAAAAACATCTAATA
ENST00000438166.6:c.1959+59_1959+60insAGAAAAACATCTAATA	ENSP00000409708.2:n.1959+59_1959+60insAGAAAAACATCTAATA
ENST00000464846.5:n.397+59_397+60insAGAAAAACATCTAATA
ENST00000492005.1:n.82+59_82+60insAGAAAAACATCTAATA
ENST00000540309.5:c.*73+59_*73+60insAGAAAAACATCTAATA	ENSP00000440892.1:n.*73+59_*73+60insAGAAAAACATCTAATA
NM_000408.4:c.1959+59_1959+60insAGAAAAACATCTAATA	NP_000399.3:n.1959+59_1959+60insAGAAAAACATCTAATA
NM_001083112.2:c.1959+59_1959+60insAGAAAAACATCTAATA	NP_001076581.2:n.1959+59_1959+60insAGAAAAACATCTAATA
XM_005246469.1:c.1959+59_1959+60insAGAAAAACATCTAATA	XP_005246526.1:n.1959+59_1959+60insAGAAAAACATCTAATA
XM_005246470.3:c.1857+59_1857+60insAGAAAAACATCTAATA	XP_005246527.1:n.1857+59_1857+60insAGAAAAACATCTAATA
XM_011510977.1:c.1959+59_1959+60insAGAAAAACATCTAATA	XP_011509279.1:n.1959+59_1959+60insAGAAAAACATCTAATA
XM_011510978.1:c.1857+59_1857+60insAGAAAAACATCTAATA	XP_011509280.1:n.1857+59_1857+60insAGAAAAACATCTAATA
XM_011510979.1:c.1581+59_1581+60insAGAAAAACATCTAATA	XP_011509281.1:n.1581+59_1581+60insAGAAAAACATCTAATA
XM_011510980.1:c.1278+59_1278+60insAGAAAAACATCTAATA	XP_011509282.1:n.1278+59_1278+60insAGAAAAACATCTAATA
XM_005246469.2:c.1959+59_1959+60insAGAAAAACATCTAATA	XP_005246526.1:n.1959+59_1959+60insAGAAAAACATCTAATA
XM_011510977.2:c.1959+59_1959+60insAGAAAAACATCTAATA	XP_011509279.1:n.1959+59_1959+60insAGAAAAACATCTAATA
XM_011510978.2:c.1857+59_1857+60insAGAAAAACATCTAATA	XP_011509280.1:n.1857+59_1857+60insAGAAAAACATCTAATA
XM_017003830.1:c.1959+59_1959+60insAGAAAAACATCTAATA	XP_016859319.1:n.1959+59_1959+60insAGAAAAACATCTAATA
XM_024452798.1:c.1959+59_1959+60insAGAAAAACATCTAATA	XP_024308566.1:n.1959+59_1959+60insAGAAAAACATCTAATA
NM_000408.5:c.1959+59_1959+60insAGAAAAACATCTAATA MANE Select	NP_000399.3:n.1959+59_1959+60insAGAAAAACATCTAATA
NM_001083112.3:c.1959+59_1959+60insAGAAAAACATCTAATA	NP_001076581.2:n.1959+59_1959+60insAGAAAAACATCTAATA