Canonical Allele Identifier: CA10088211

Gene: ADA2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17207064T>C , CM000684.2:g.17207064T>C	GRCh38
NC_000022.10:g.17687954T>C , CM000684.1:g.17687954T>C	GRCh37
NC_000022.9:g.16067954T>C	NCBI36
NG_033943.1:g.19791A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449907.8:c.416+7A>G	ENSP00000406443.2:n.416+7A>G
ENST00000543038.2:c.542+7A>G	ENSP00000442482.2:n.542+7A>G
ENST00000610390.5:c.182+7A>G	ENSP00000483418.1:n.182+7A>G
ENST00000649310.2:c.542+7A>G	ENSP00000496839.2:n.542+7A>G
ENST00000649746.2:c.542+7A>G	ENSP00000497913.2:n.542+7A>G
ENST00000649915.2:c.542+7A>G	ENSP00000497681.2:n.542+7A>G
ENST00000696196.1:c.542+7A>G	ENSP00000512479.1:n.542+7A>G
ENST00000696197.1:c.542+7A>G	ENSP00000512480.1:n.542+7A>G
ENST00000696225.1:c.542+7A>G	ENSP00000512491.1:n.542+7A>G
ENST00000696226.1:c.542+7A>G	ENSP00000512492.1:n.542+7A>G
ENST00000696227.1:c.542+7A>G	ENSP00000512493.1:n.542+7A>G
ENST00000399837.8:c.542+7A>G MANE Select	ENSP00000382731.2:n.542+7A>G
ENST00000449907.7:c.416+7A>G	ENSP00000406443.2:n.416+7A>G
ENST00000649540.1:c.416+7A>G	ENSP00000497469.1:n.416+7A>G
ENST00000649915.1:c.369+7A>G
ENST00000650635.1:n.542+7A>G
ENST00000262607.3:c.542+7A>G	ENSP00000262607.2:n.542+7A>G
ENST00000399837.6:c.542+7A>G	ENSP00000382731.2:n.542+7A>G
ENST00000399839.5:c.542+7A>G	ENSP00000382733.1:n.542+7A>G
ENST00000449907.6:c.416+7A>G	ENSP00000406443.2:n.416+7A>G
ENST00000610390.4:c.182+7A>G	ENSP00000483418.1:n.182+7A>G
NM_001282225.1:c.542+7A>G	NP_001269154.1:n.542+7A>G
NM_001282226.1:c.542+7A>G	NP_001269155.1:n.542+7A>G
NM_001282227.1:c.416+7A>G	NP_001269156.1:n.416+7A>G
NM_001282228.1:c.416+7A>G	NP_001269157.1:n.416+7A>G
NM_001282229.1:c.182+7A>G	NP_001269158.1:n.182+7A>G
XM_006724080.2:c.-1829+7A>G	XP_006724143.1:n.-1829+7A>G
XM_011546133.1:c.542+7A>G	XP_011544435.1:n.542+7A>G
NM_001282225.2:c.542+7A>G MANE Select	NP_001269154.1:n.542+7A>G
XM_006724080.3:c.-1829+7A>G	XP_006724143.1:n.-1829+7A>G
XM_011546133.2:c.542+7A>G	XP_011544435.1:n.542+7A>G
NM_001282226.2:c.542+7A>G	NP_001269155.1:n.542+7A>G
NM_001282227.2:c.416+7A>G	NP_001269156.1:n.416+7A>G
NM_001282228.2:c.416+7A>G	NP_001269157.1:n.416+7A>G
NM_001282229.2:c.182+7A>G	NP_001269158.1:n.182+7A>G