Canonical Allele Identifier: CA410231167

Gene: ADA2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17209639G>T , CM000684.2:g.17209639G>T	GRCh38
NC_000022.10:g.17690529G>T , CM000684.1:g.17690529G>T	GRCh37
NC_000022.9:g.16070529G>T	NCBI36
NG_033943.1:g.17216C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001282225.2:c.39C>A MANE Select	NP_001269154.1:p.Cys13Ter
ENST00000399837.8:c.39C>A MANE Select	ENSP00000382731.2:p.Cys13Ter
NM_001282225.1:c.39C>A	NP_001269154.1:p.Cys13Ter
NM_001282226.1:c.39C>A	NP_001269155.1:p.Cys13Ter
NM_001282226.2:c.39C>A	NP_001269155.1:p.Cys13Ter
NM_001282227.1:c.-47-41C>A	NP_001269156.1:n.-47-41C>A
NM_001282227.2:c.-47-41C>A	NP_001269156.1:n.-47-41C>A
NM_001282228.1:c.-47-41C>A	NP_001269157.1:n.-47-41C>A
NM_001282228.2:c.-47-41C>A	NP_001269157.1:n.-47-41C>A
NM_001282229.1:c.-38-2349C>A	NP_001269158.1:n.-38-2349C>A
NM_001282229.2:c.-38-2349C>A	NP_001269158.1:n.-38-2349C>A
ENST00000262607.3:c.39C>A	ENSP00000262607.2:p.Cys13Ter
ENST00000399837.6:c.39C>A	ENSP00000382731.2:p.Cys13Ter
ENST00000399839.5:c.39C>A	ENSP00000382733.1:p.Cys13Ter
ENST00000441548.1:c.39C>A	ENSP00000392078.1:p.Cys13Ter
ENST00000449907.6:c.-47-41C>A	ENSP00000406443.2:n.-47-41C>A
ENST00000449907.7:c.-47-41C>A	ENSP00000406443.2:n.-47-41C>A
ENST00000449907.8:c.-47-41C>A	ENSP00000406443.2:n.-47-41C>A
ENST00000543038.1:c.39C>A	ENSP00000442482.1:p.Cys13Ter
ENST00000543038.2:c.39C>A	ENSP00000442482.2:p.Cys13Ter
ENST00000610390.4:c.-38-2349C>A	ENSP00000483418.1:n.-38-2349C>A
ENST00000610390.5:c.-38-2349C>A	ENSP00000483418.1:n.-38-2349C>A
ENST00000649310.1:c.39C>A	ENSP00000496839.1:p.Cys13Ter
ENST00000649310.2:c.39C>A	ENSP00000496839.2:p.Cys13Ter
ENST00000649540.1:c.-47-41C>A	ENSP00000497469.1:n.-47-41C>A
ENST00000649746.1:c.39C>A	ENSP00000497913.1:p.Cys13Ter
ENST00000649746.2:c.39C>A	ENSP00000497913.2:p.Cys13Ter
ENST00000649915.2:c.39C>A	ENSP00000497681.2:p.Cys13Ter
ENST00000650635.1:n.80-41C>A
ENST00000696196.1:c.39C>A	ENSP00000512479.1:p.Cys13Ter
ENST00000696197.1:c.39C>A	ENSP00000512480.1:p.Cys13Ter
ENST00000696225.1:c.39C>A	ENSP00000512491.1:p.Cys13Ter
ENST00000696226.1:c.39C>A	ENSP00000512492.1:p.Cys13Ter
ENST00000696227.1:c.39C>A	ENSP00000512493.1:p.Cys13Ter
XM_011546133.1:c.39C>A	XP_011544435.1:p.Cys13Ter
XM_011546133.2:c.39C>A	XP_011544435.1:p.Cys13Ter