Canonical Allele Identifier: CA2661544727

Gene: GPD2

Linked Data

• gnomAD v4: 2-156579031-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579039_156579040dup , CM000664.2:g.156579039_156579040dup	GRCh38
NC_000002.11:g.157435551_157435552dup , CM000664.1:g.157435551_157435552dup	GRCh37
NC_000002.10:g.157143797_157143798dup	NCBI36
NG_016606.1:g.148587_148588dup
NG_016606.2:g.148587_148588dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1880+38_1880+39dup MANE Select	ENSP00000409708.2:n.1880+38_1880+39dup
ENST00000310454.10:c.1880+38_1880+39dup	ENSP00000308610.5:n.1880+38_1880+39dup
ENST00000409125.8:c.1502+38_1502+39dup	ENSP00000386484.5:n.1502+38_1502+39dup
ENST00000409674.5:c.1880+38_1880+39dup	ENSP00000386425.1:n.1880+38_1880+39dup
ENST00000409861.5:c.1880+38_1880+39dup	ENSP00000386626.1:n.1880+38_1880+39dup
ENST00000438166.6:c.1880+38_1880+39dup	ENSP00000409708.2:n.1880+38_1880+39dup
ENST00000464846.5:n.272_273dup
ENST00000540309.5:c.1135-47_1135-46dup	ENSP00000440892.1:n.1135-47_1135-46dup
NM_000408.4:c.1880+38_1880+39dup	NP_000399.3:n.1880+38_1880+39dup
NM_001083112.2:c.1880+38_1880+39dup	NP_001076581.2:n.1880+38_1880+39dup
XM_005246469.1:c.1880+38_1880+39dup	XP_005246526.1:n.1880+38_1880+39dup
XM_005246470.3:c.1778+38_1778+39dup	XP_005246527.1:n.1778+38_1778+39dup
XM_011510977.1:c.1880+38_1880+39dup	XP_011509279.1:n.1880+38_1880+39dup
XM_011510978.1:c.1778+38_1778+39dup	XP_011509280.1:n.1778+38_1778+39dup
XM_011510979.1:c.1502+38_1502+39dup	XP_011509281.1:n.1502+38_1502+39dup
XM_011510980.1:c.1199+38_1199+39dup	XP_011509282.1:n.1199+38_1199+39dup
XM_005246469.2:c.1880+38_1880+39dup	XP_005246526.1:n.1880+38_1880+39dup
XM_011510977.2:c.1880+38_1880+39dup	XP_011509279.1:n.1880+38_1880+39dup
XM_011510978.2:c.1778+38_1778+39dup	XP_011509280.1:n.1778+38_1778+39dup
XM_017003830.1:c.1880+38_1880+39dup	XP_016859319.1:n.1880+38_1880+39dup
XM_024452798.1:c.1880+38_1880+39dup	XP_024308566.1:n.1880+38_1880+39dup
NM_000408.5:c.1880+38_1880+39dup MANE Select	NP_000399.3:n.1880+38_1880+39dup
NM_001083112.3:c.1880+38_1880+39dup	NP_001076581.2:n.1880+38_1880+39dup