Canonical Allele Identifier: CA348664844

Gene: GPD2

Linked Data

• MyVariant Identifiers: chr2:g.157435641T>G (hg19) ; chr2:g.156579129T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579129T>G , CM000664.2:g.156579129T>G	GRCh38
NC_000002.11:g.157435641T>G , CM000664.1:g.157435641T>G	GRCh37
NC_000002.10:g.157143887T>G	NCBI36
NG_016606.1:g.148677T>G
NG_016606.2:g.148677T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1924T>G MANE Select	ENSP00000409708.2:p.Phe642Val
ENST00000310454.10:c.1924T>G	ENSP00000308610.5:p.Phe642Val
ENST00000409125.8:c.1546T>G	ENSP00000386484.5:p.Phe516Val
ENST00000409674.5:c.1924T>G	ENSP00000386425.1:p.Phe642Val
ENST00000409861.5:c.1924T>G	ENSP00000386626.1:p.Phe642Val
ENST00000438166.6:c.1924T>G	ENSP00000409708.2:p.Phe642Val
ENST00000464846.5:n.362T>G
ENST00000492005.1:n.47T>G
ENST00000540309.5:c.*38T>G	ENSP00000440892.1:n.*38T>G
NM_000408.4:c.1924T>G	NP_000399.3:p.Phe642Val
NM_001083112.2:c.1924T>G	NP_001076581.2:p.Phe642Val
XM_005246469.1:c.1924T>G	XP_005246526.1:p.Phe642Val
XM_005246470.3:c.1822T>G	XP_005246527.1:p.Phe608Val
XM_011510977.1:c.1924T>G	XP_011509279.1:p.Phe642Val
XM_011510978.1:c.1822T>G	XP_011509280.1:p.Phe608Val
XM_011510979.1:c.1546T>G	XP_011509281.1:p.Phe516Val
XM_011510980.1:c.1243T>G	XP_011509282.1:p.Phe415Val
XM_005246469.2:c.1924T>G	XP_005246526.1:p.Phe642Val
XM_011510977.2:c.1924T>G	XP_011509279.1:p.Phe642Val
XM_011510978.2:c.1822T>G	XP_011509280.1:p.Phe608Val
XM_017003830.1:c.1924T>G	XP_016859319.1:p.Phe642Val
XM_024452798.1:c.1924T>G	XP_024308566.1:p.Phe642Val
NM_000408.5:c.1924T>G MANE Select	NP_000399.3:p.Phe642Val
NM_001083112.3:c.1924T>G	NP_001076581.2:p.Phe642Val