Canonical Allele Identifier: CA410233181

Gene: ADA2

Linked Data

• COSMIC: COSM725680 ; COSM1149409
• MyVariant Identifiers: chr22:g.17669238C>G (hg19) ; chr22:g.17188348C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17188348C>G , CM000684.2:g.17188348C>G	GRCh38
NC_000022.10:g.17669238C>G , CM000684.1:g.17669238C>G	GRCh37
NC_000022.9:g.16049238C>G	NCBI36
NG_033943.1:g.38507G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330232.9:c.349G>C	ENSP00000332871.4:p.Gly117Arg
ENST00000449907.8:c.946G>C	ENSP00000406443.2:p.Gly316Arg
ENST00000469063.2:n.960G>C
ENST00000543038.2:c.1072G>C	ENSP00000442482.2:p.Gly358Arg
ENST00000610390.5:c.712G>C	ENSP00000483418.1:p.Gly238Arg
ENST00000648061.2:c.*48G>C	ENSP00000496894.1:n.*48G>C
ENST00000649310.2:c.1072G>C	ENSP00000496839.2:p.Gly358Arg
ENST00000649746.2:c.1072G>C	ENSP00000497913.2:p.Gly358Arg
ENST00000649915.2:c.*2194G>C	ENSP00000497681.2:n.*2194G>C
ENST00000696189.1:n.373G>C
ENST00000696196.1:c.1072G>C	ENSP00000512479.1:p.Gly358Arg
ENST00000696197.1:c.1072G>C	ENSP00000512480.1:p.Gly358Arg
ENST00000696218.1:n.184G>C
ENST00000696220.1:c.319G>C	ENSP00000512486.1:p.Gly107Arg
ENST00000696221.1:c.319G>C	ENSP00000512487.1:p.Gly107Arg
ENST00000696222.1:c.319G>C	ENSP00000512488.1:p.Gly107Arg
ENST00000696223.1:c.319G>C	ENSP00000512489.1:p.Gly107Arg
ENST00000696224.1:c.466G>C	ENSP00000512490.1:p.Gly156Arg
ENST00000696225.1:c.1072G>C	ENSP00000512491.1:p.Gly358Arg
ENST00000399837.8:c.1072G>C MANE Select	ENSP00000382731.2:p.Gly358Arg
ENST00000449907.7:c.946G>C	ENSP00000406443.2:p.Gly316Arg
ENST00000648061.1:c.*48G>C	ENSP00000496894.1:n.*48G>C
ENST00000648668.1:n.510G>C
ENST00000649540.1:c.946G>C	ENSP00000497469.1:p.Gly316Arg
ENST00000649915.1:c.2585G>C
ENST00000262607.3:c.1072G>C	ENSP00000262607.2:p.Gly358Arg
ENST00000330232.8:c.349G>C	ENSP00000332871.4:p.Gly117Arg
ENST00000399837.6:c.1072G>C	ENSP00000382731.2:p.Gly358Arg
ENST00000399839.5:c.1072G>C	ENSP00000382733.1:p.Gly358Arg
ENST00000449907.6:c.946G>C	ENSP00000406443.2:p.Gly316Arg
ENST00000469063.1:n.380G>C
ENST00000610390.4:c.712G>C	ENSP00000483418.1:p.Gly238Arg
NM_001282225.1:c.1072G>C	NP_001269154.1:p.Gly358Arg
NM_001282226.1:c.1072G>C	NP_001269155.1:p.Gly358Arg
NM_001282227.1:c.946G>C	NP_001269156.1:p.Gly316Arg
NM_001282228.1:c.946G>C	NP_001269157.1:p.Gly316Arg
NM_001282229.1:c.712G>C	NP_001269158.1:p.Gly238Arg
NM_177405.2:c.349G>C	NP_803124.1:p.Gly117Arg
XM_006724080.2:c.388G>C	XP_006724143.1:p.Gly130Arg
XM_011546133.1:c.1072G>C	XP_011544435.1:p.Gly358Arg
NM_001282225.2:c.1072G>C MANE Select	NP_001269154.1:p.Gly358Arg
XM_006724080.3:c.388G>C	XP_006724143.1:p.Gly130Arg
XM_011546133.2:c.1072G>C	XP_011544435.1:p.Gly358Arg
NM_001282226.2:c.1072G>C	NP_001269155.1:p.Gly358Arg
NM_001282227.2:c.946G>C	NP_001269156.1:p.Gly316Arg
NM_001282228.2:c.946G>C	NP_001269157.1:p.Gly316Arg
NM_177405.3:c.349G>C	NP_803124.1:p.Gly117Arg
NM_001282229.2:c.712G>C	NP_001269158.1:p.Gly238Arg