Canonical Allele Identifier: CA1917116

Gene: GPD2

Linked Data

• dbSNP Id: rs763866949
• ExAC: 2:157435518 T / TTA
• gnomAD v2: 2-157435518-T-TTA
• gnomAD v3: 2-156579006-T-TTA
• gnomAD v4: 2-156579006-T-TTA
• MyVariant Identifiers: chr2:g.157435518_157435519insTA (hg19) ; chr2:g.156579006_156579007insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579009_156579010dup , CM000664.2:g.156579009_156579010dup	GRCh38
NC_000002.11:g.157435521_157435522dup , CM000664.1:g.157435521_157435522dup	GRCh37
NC_000002.10:g.157143767_157143768dup	NCBI36
NG_016606.1:g.148557_148558dup
NG_016606.2:g.148557_148558dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1880+8_1880+9dup MANE Select	ENSP00000409708.2:n.1880+8_1880+9dup
ENST00000310454.10:c.1880+8_1880+9dup	ENSP00000308610.5:n.1880+8_1880+9dup
ENST00000409125.8:c.1502+8_1502+9dup	ENSP00000386484.5:n.1502+8_1502+9dup
ENST00000409674.5:c.1880+8_1880+9dup	ENSP00000386425.1:n.1880+8_1880+9dup
ENST00000409861.5:c.1880+8_1880+9dup	ENSP00000386626.1:n.1880+8_1880+9dup
ENST00000438166.6:c.1880+8_1880+9dup	ENSP00000409708.2:n.1880+8_1880+9dup
ENST00000464846.5:n.242_243dup
ENST00000540309.5:c.1135-77_1135-76dup	ENSP00000440892.1:n.1135-77_1135-76dup
NM_000408.4:c.1880+8_1880+9dup	NP_000399.3:n.1880+8_1880+9dup
NM_001083112.2:c.1880+8_1880+9dup	NP_001076581.2:n.1880+8_1880+9dup
XM_005246469.1:c.1880+8_1880+9dup	XP_005246526.1:n.1880+8_1880+9dup
XM_005246470.3:c.1778+8_1778+9dup	XP_005246527.1:n.1778+8_1778+9dup
XM_011510977.1:c.1880+8_1880+9dup	XP_011509279.1:n.1880+8_1880+9dup
XM_011510978.1:c.1778+8_1778+9dup	XP_011509280.1:n.1778+8_1778+9dup
XM_011510979.1:c.1502+8_1502+9dup	XP_011509281.1:n.1502+8_1502+9dup
XM_011510980.1:c.1199+8_1199+9dup	XP_011509282.1:n.1199+8_1199+9dup
XM_005246469.2:c.1880+8_1880+9dup	XP_005246526.1:n.1880+8_1880+9dup
XM_011510977.2:c.1880+8_1880+9dup	XP_011509279.1:n.1880+8_1880+9dup
XM_011510978.2:c.1778+8_1778+9dup	XP_011509280.1:n.1778+8_1778+9dup
XM_017003830.1:c.1880+8_1880+9dup	XP_016859319.1:n.1880+8_1880+9dup
XM_024452798.1:c.1880+8_1880+9dup	XP_024308566.1:n.1880+8_1880+9dup
NM_000408.5:c.1880+8_1880+9dup MANE Select	NP_000399.3:n.1880+8_1880+9dup
NM_001083112.3:c.1880+8_1880+9dup	NP_001076581.2:n.1880+8_1880+9dup