Canonical Allele Identifier: CA1300570931

Gene: GPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579109T= , CM000664.2:g.156579109T=	GRCh38
NC_000002.11:g.157435621T= , CM000664.1:g.157435621T=	GRCh37
NC_000002.10:g.157143867T=	NCBI36
NG_016606.1:g.148657T=
NG_016606.2:g.148657T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1904T= MANE Select	ENSP00000409708.2:p.Phe635=
ENST00000310454.10:c.1904T=	ENSP00000308610.5:p.Phe635=
ENST00000409125.8:c.1526T=	ENSP00000386484.5:p.Phe509=
ENST00000409674.5:c.1904T=	ENSP00000386425.1:p.Phe635=
ENST00000409861.5:c.1904T=	ENSP00000386626.1:p.Phe635=
ENST00000438166.6:c.1904T=	ENSP00000409708.2:p.Phe635=
ENST00000464846.5:n.342T=
ENST00000492005.1:n.27T=
ENST00000540309.5:c.*18T=	ENSP00000440892.1:n.*18T=
NM_000408.4:c.1904T=	NP_000399.3:p.Phe635=
NM_001083112.2:c.1904T=	NP_001076581.2:p.Phe635=
XM_005246469.1:c.1904T=	XP_005246526.1:p.Phe635=
XM_005246470.3:c.1802T=	XP_005246527.1:p.Phe601=
XM_011510977.1:c.1904T=	XP_011509279.1:p.Phe635=
XM_011510978.1:c.1802T=	XP_011509280.1:p.Phe601=
XM_011510979.1:c.1526T=	XP_011509281.1:p.Phe509=
XM_011510980.1:c.1223T=	XP_011509282.1:p.Phe408=
XM_005246469.2:c.1904T=	XP_005246526.1:p.Phe635=
XM_011510977.2:c.1904T=	XP_011509279.1:p.Phe635=
XM_011510978.2:c.1802T=	XP_011509280.1:p.Phe601=
XM_017003830.1:c.1904T=	XP_016859319.1:p.Phe635=
XM_024452798.1:c.1904T=	XP_024308566.1:p.Phe635=
NM_000408.5:c.1904T= MANE Select	NP_000399.3:p.Phe635=
NM_001083112.3:c.1904T=	NP_001076581.2:p.Phe635=