Canonical Allele Identifier: CA1300570849

Gene: GPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156578946T= , CM000664.2:g.156578946T=	GRCh38
NC_000002.11:g.157435458T= , CM000664.1:g.157435458T=	GRCh37
NC_000002.10:g.157143704T=	NCBI36
NG_016606.1:g.148494T=
NG_016606.2:g.148494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1825T= MANE Select	ENSP00000409708.2:p.Ser609=
ENST00000310454.10:c.1825T=	ENSP00000308610.5:p.Ser609=
ENST00000409125.8:c.1447T=	ENSP00000386484.5:p.Ser483=
ENST00000409674.5:c.1825T=	ENSP00000386425.1:p.Ser609=
ENST00000409861.5:c.1825T=	ENSP00000386626.1:p.Ser609=
ENST00000438166.6:c.1825T=	ENSP00000409708.2:p.Ser609=
ENST00000464846.5:n.179T=
ENST00000540309.5:c.1135-140T=	ENSP00000440892.1:n.1135-140T=
NM_000408.4:c.1825T=	NP_000399.3:p.Ser609=
NM_001083112.2:c.1825T=	NP_001076581.2:p.Ser609=
XM_005246469.1:c.1825T=	XP_005246526.1:p.Ser609=
XM_005246470.3:c.1723T=	XP_005246527.1:p.Ser575=
XM_011510977.1:c.1825T=	XP_011509279.1:p.Ser609=
XM_011510978.1:c.1723T=	XP_011509280.1:p.Ser575=
XM_011510979.1:c.1447T=	XP_011509281.1:p.Ser483=
XM_011510980.1:c.1144T=	XP_011509282.1:p.Ser382=
XM_005246469.2:c.1825T=	XP_005246526.1:p.Ser609=
XM_011510977.2:c.1825T=	XP_011509279.1:p.Ser609=
XM_011510978.2:c.1723T=	XP_011509280.1:p.Ser575=
XM_017003830.1:c.1825T=	XP_016859319.1:p.Ser609=
XM_024452798.1:c.1825T=	XP_024308566.1:p.Ser609=
NM_000408.5:c.1825T= MANE Select	NP_000399.3:p.Ser609=
NM_001083112.3:c.1825T=	NP_001076581.2:p.Ser609=