Canonical Allele Identifier: CA385299572

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56475655C>T , CM000674.2:g.56475655C>T GRCh38
NC_000012.11:g.56869439C>T , CM000674.1:g.56869439C>T GRCh37
NC_000012.10:g.55155706C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_013267.4:c.898G>A (GLS2) MANE Select NP_037399.2:p.Gly300Arg
NM_207344.4:c.*6078C>T (SPRYD4) MANE Select NP_997227.1:n.*6078C>T
ENST00000311966.9:c.898G>A (GLS2) MANE Select ENSP00000310447.4:p.Gly300Arg
ENST00000338146.7:c.*6078C>T (SPRYD4) MANE Select ENSP00000338034.5:n.*6078C>T
NM_001280796.1:c.-4G>A (GLS2) NP_001267725.1:n.-4G>A
NM_001280796.2:c.-4G>A (GLS2) NP_001267725.1:n.-4G>A
NM_001280797.1:c.103G>A (GLS2) NP_001267726.1:p.Gly35Arg
NM_001280797.2:c.103G>A (GLS2) NP_001267726.1:p.Gly35Arg
NM_001280798.1:c.103G>A (GLS2) NP_001267727.1:p.Gly35Arg
NM_001280798.2:c.103G>A (GLS2) NP_001267727.1:p.Gly35Arg
NM_013267.3:c.898G>A (GLS2) NP_037399.2:p.Gly300Arg
ENST00000311966.8:c.898G>A (GLS2) ENSP00000310447.4:p.Gly300Arg
ENST00000338146.6:c.*6078C>T (SPRYD4) ENSP00000338034.5:n.*6078C>T
ENST00000424141.6:c.*234G>A (GLS2) ENSP00000416282.2:n.*234G>A
ENST00000461077.1:c.465G>A (GLS2) ENSP00000417244.1:p.Leu155=
ENST00000476991.5:n.135G>A (GLS2)
ENST00000479952.5:c.432G>A (GLS2) ENSP00000417796.1:p.Leu144=
ENST00000486433.5:c.898G>A (GLS2) ENSP00000420328.1:p.Gly300Arg
ENST00000486896.5:c.*496G>A (GLS2) ENSP00000419661.1:n.*496G>A
ENST00000494474.5:c.*234G>A (GLS2) ENSP00000419996.1:n.*234G>A
ENST00000496006.5:n.102G>A (GLS2)
ENST00000539272.5:c.787G>A (GLS2) ENSP00000441739.2:p.Gly263Arg
ENST00000610413.4:c.103G>A (GLS2) ENSP00000483010.1:p.Gly35Arg
ENST00000623608.3:c.103G>A (GLS2) ENSP00000485315.1:p.Gly35Arg
ENST00000648304.1:c.182+12282G>A ENSP00000497190.1:n.182+12282G>A
XM_005268797.1:c.790G>A (GLS2) XP_005268854.1:p.Gly264Arg
XM_017019180.1:c.103G>A (GLS2) XP_016874669.1:p.Gly35Arg