Canonical Allele Identifier: CA6632857

Gene: GLS2 SPRYD4

Linked Data

• dbSNP Id: rs2657879
• ExAC: 12:56865338 A / G
• gnomAD v2: 12-56865338-A-G
• gnomAD v3: 12-56471554-A-G
• gnomAD v4: 12-56471554-A-G
• MyVariant Identifiers: chr12:g.56865338A>G (hg19) ; chr12:g.56471554A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56471554A>G , CM000674.2:g.56471554A>G	GRCh38
NC_000012.11:g.56865338A>G , CM000674.1:g.56865338A>G	GRCh37
NC_000012.10:g.55151605A>G	NCBI36
NG_021397.2:g.2613T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000311966.9:c.1742T>C (GLS2) MANE Select	ENSP00000310447.4:p.Leu581Pro
ENST00000338146.7:c.*1977A>G (SPRYD4) MANE Select	ENSP00000338034.5:n.*1977A>G
ENST00000648304.1:c.182+16383T>C	ENSP00000497190.1:n.182+16383T>C
ENST00000311966.8:c.1742T>C (GLS2)	ENSP00000310447.4:p.Leu581Pro
ENST00000338146.6:c.*1977A>G (SPRYD4)	ENSP00000338034.5:n.*1977A>G
ENST00000390288.6:n.790T>C (GLS2)
ENST00000424141.6:c.*1078T>C (GLS2)	ENSP00000416282.2:n.*1078T>C
ENST00000479952.5:c.*735T>C (GLS2)	ENSP00000417796.1:n.*735T>C
ENST00000486433.5:c.*831T>C (GLS2)	ENSP00000420328.1:n.*831T>C
ENST00000539272.5:c.1564T>C (GLS2)	ENSP00000441739.2:n.1564T>C
ENST00000610413.4:c.947T>C (GLS2)	ENSP00000483010.1:p.Leu316Pro
ENST00000623608.3:c.947T>C (GLS2)	ENSP00000485315.1:p.Leu316Pro
NM_001280796.1:c.914T>C (GLS2)	NP_001267725.1:p.Leu305Pro
NM_001280797.1:c.947T>C (GLS2)	NP_001267726.1:p.Leu316Pro
NM_001280798.1:c.947T>C (GLS2)	NP_001267727.1:p.Leu316Pro
NM_013267.3:c.1742T>C (GLS2)	NP_037399.2:p.Leu581Pro
XM_005268797.1:c.1634T>C (GLS2)	XP_005268854.1:p.Leu545Pro
XM_017019180.1:c.947T>C (GLS2)	XP_016874669.1:p.Leu316Pro
NM_013267.4:c.1742T>C (GLS2) MANE Select	NP_037399.2:p.Leu581Pro
NM_207344.4:c.*1977A>G (SPRYD4) MANE Select	NP_997227.1:n.*1977A>G
NM_001280796.2:c.914T>C (GLS2)	NP_001267725.1:p.Leu305Pro
NM_001280797.2:c.947T>C (GLS2)	NP_001267726.1:p.Leu316Pro
NM_001280798.2:c.947T>C (GLS2)	NP_001267727.1:p.Leu316Pro