Canonical Allele Identifier: CA1300570818

Gene: GPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156578880_156578882delinsCTG , CM000664.2:g.156578880_156578882delinsCTG	GRCh38
NC_000002.11:g.157435392_157435394delinsCTG , CM000664.1:g.157435392_157435394delinsCTG	GRCh37
NC_000002.10:g.157143638_157143640delinsCTG	NCBI36
NG_016606.1:g.148428_148430delinsCTG
NG_016606.2:g.148428_148430delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1768-9_1768-7delinsCTG MANE Select	ENSP00000409708.2:n.1768-9_1768-7delinsCTG
ENST00000310454.10:c.1768-9_1768-7delinsCTG	ENSP00000308610.5:n.1768-9_1768-7delinsCTG
ENST00000409125.8:c.1390-9_1390-7delinsCTG	ENSP00000386484.5:n.1390-9_1390-7delinsCTG
ENST00000409674.5:c.1768-9_1768-7delinsCTG	ENSP00000386425.1:n.1768-9_1768-7delinsCTG
ENST00000409861.5:c.1768-9_1768-7delinsCTG	ENSP00000386626.1:n.1768-9_1768-7delinsCTG
ENST00000438166.6:c.1768-9_1768-7delinsCTG	ENSP00000409708.2:n.1768-9_1768-7delinsCTG
ENST00000464846.5:n.122-9_122-7delinsCTG
ENST00000540309.5:c.1135-206_1135-204delinsCTG	ENSP00000440892.1:n.1135-206_1135-204delinsCTG
NM_000408.4:c.1768-9_1768-7delinsCTG	NP_000399.3:n.1768-9_1768-7delinsCTG
NM_001083112.2:c.1768-9_1768-7delinsCTG	NP_001076581.2:n.1768-9_1768-7delinsCTG
XM_005246469.1:c.1768-9_1768-7delinsCTG	XP_005246526.1:n.1768-9_1768-7delinsCTG
XM_005246470.3:c.1666-9_1666-7delinsCTG	XP_005246527.1:n.1666-9_1666-7delinsCTG
XM_011510977.1:c.1768-9_1768-7delinsCTG	XP_011509279.1:n.1768-9_1768-7delinsCTG
XM_011510978.1:c.1666-9_1666-7delinsCTG	XP_011509280.1:n.1666-9_1666-7delinsCTG
XM_011510979.1:c.1390-9_1390-7delinsCTG	XP_011509281.1:n.1390-9_1390-7delinsCTG
XM_011510980.1:c.1087-9_1087-7delinsCTG	XP_011509282.1:n.1087-9_1087-7delinsCTG
XM_005246469.2:c.1768-9_1768-7delinsCTG	XP_005246526.1:n.1768-9_1768-7delinsCTG
XM_011510977.2:c.1768-9_1768-7delinsCTG	XP_011509279.1:n.1768-9_1768-7delinsCTG
XM_011510978.2:c.1666-9_1666-7delinsCTG	XP_011509280.1:n.1666-9_1666-7delinsCTG
XM_017003830.1:c.1768-9_1768-7delinsCTG	XP_016859319.1:n.1768-9_1768-7delinsCTG
XM_024452798.1:c.1768-9_1768-7delinsCTG	XP_024308566.1:n.1768-9_1768-7delinsCTG
NM_000408.5:c.1768-9_1768-7delinsCTG MANE Select	NP_000399.3:n.1768-9_1768-7delinsCTG
NM_001083112.3:c.1768-9_1768-7delinsCTG	NP_001076581.2:n.1768-9_1768-7delinsCTG