Canonical Allele Identifier: CA348664769

Gene: GPD2

Linked Data

• gnomAD v4: 2-156579115-C-T
• MyVariant Identifiers: chr2:g.157435627C>T (hg19) ; chr2:g.156579115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156579115C>T , CM000664.2:g.156579115C>T	GRCh38
NC_000002.11:g.157435627C>T , CM000664.1:g.157435627C>T	GRCh37
NC_000002.10:g.157143873C>T	NCBI36
NG_016606.1:g.148663C>T
NG_016606.2:g.148663C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438166.7:c.1910C>T MANE Select	ENSP00000409708.2:p.Ala637Val
ENST00000310454.10:c.1910C>T	ENSP00000308610.5:p.Ala637Val
ENST00000409125.8:c.1532C>T	ENSP00000386484.5:p.Ala511Val
ENST00000409674.5:c.1910C>T	ENSP00000386425.1:p.Ala637Val
ENST00000409861.5:c.1910C>T	ENSP00000386626.1:p.Ala637Val
ENST00000438166.6:c.1910C>T	ENSP00000409708.2:p.Ala637Val
ENST00000464846.5:n.348C>T
ENST00000492005.1:n.33C>T
ENST00000540309.5:c.*24C>T	ENSP00000440892.1:n.*24C>T
NM_000408.4:c.1910C>T	NP_000399.3:p.Ala637Val
NM_001083112.2:c.1910C>T	NP_001076581.2:p.Ala637Val
XM_005246469.1:c.1910C>T	XP_005246526.1:p.Ala637Val
XM_005246470.3:c.1808C>T	XP_005246527.1:p.Ala603Val
XM_011510977.1:c.1910C>T	XP_011509279.1:p.Ala637Val
XM_011510978.1:c.1808C>T	XP_011509280.1:p.Ala603Val
XM_011510979.1:c.1532C>T	XP_011509281.1:p.Ala511Val
XM_011510980.1:c.1229C>T	XP_011509282.1:p.Ala410Val
XM_005246469.2:c.1910C>T	XP_005246526.1:p.Ala637Val
XM_011510977.2:c.1910C>T	XP_011509279.1:p.Ala637Val
XM_011510978.2:c.1808C>T	XP_011509280.1:p.Ala603Val
XM_017003830.1:c.1910C>T	XP_016859319.1:p.Ala637Val
XM_024452798.1:c.1910C>T	XP_024308566.1:p.Ala637Val
NM_000408.5:c.1910C>T MANE Select	NP_000399.3:p.Ala637Val
NM_001083112.3:c.1910C>T	NP_001076581.2:p.Ala637Val