Canonical Allele Identifier: CA410227757
Community Standard Title: NM_001282225.2(ADA2):c.753+2T>A
Gene: ADA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17203561A>T , CM000684.2:g.17203561A>T GRCh38
NC_000022.10:g.17684451A>T , CM000684.1:g.17684451A>T GRCh37
NC_000022.9:g.16064451A>T NCBI36
NG_033943.1:g.23294T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001282225.2:c.753+2T>A MANE Select NP_001269154.1:n.753+2T>A
ENST00000399837.8:c.753+2T>A MANE Select ENSP00000382731.2:n.753+2T>A
NM_001282225.1:c.753+2T>A NP_001269154.1:n.753+2T>A
NM_001282226.1:c.753+2T>A NP_001269155.1:n.753+2T>A
NM_001282226.2:c.753+2T>A NP_001269155.1:n.753+2T>A
NM_001282227.1:c.627+2T>A NP_001269156.1:n.627+2T>A
NM_001282227.2:c.627+2T>A NP_001269156.1:n.627+2T>A
NM_001282228.1:c.627+2T>A NP_001269157.1:n.627+2T>A
NM_001282228.2:c.627+2T>A NP_001269157.1:n.627+2T>A
NM_001282229.1:c.393+2T>A NP_001269158.1:n.393+2T>A
NM_001282229.2:c.393+2T>A NP_001269158.1:n.393+2T>A
ENST00000262607.3:c.753+2T>A ENSP00000262607.2:n.753+2T>A
ENST00000399837.6:c.753+2T>A ENSP00000382731.2:n.753+2T>A
ENST00000399839.5:c.753+2T>A ENSP00000382733.1:n.753+2T>A
ENST00000449907.6:c.627+2T>A ENSP00000406443.2:n.627+2T>A
ENST00000449907.7:c.627+2T>A ENSP00000406443.2:n.627+2T>A
ENST00000449907.8:c.627+2T>A ENSP00000406443.2:n.627+2T>A
ENST00000543038.2:c.753+2T>A ENSP00000442482.2:n.753+2T>A
ENST00000610390.4:c.393+2T>A ENSP00000483418.1:n.393+2T>A
ENST00000610390.5:c.393+2T>A ENSP00000483418.1:n.393+2T>A
ENST00000649310.2:c.753+2T>A ENSP00000496839.2:n.753+2T>A
ENST00000649540.1:c.627+2T>A ENSP00000497469.1:n.627+2T>A
ENST00000649746.2:c.753+2T>A ENSP00000497913.2:n.753+2T>A
ENST00000649915.1:c.616+2T>A
ENST00000649915.2:c.*225+2T>A ENSP00000497681.2:n.*225+2T>A
ENST00000650635.1:n.753+2T>A
ENST00000696196.1:c.753+2T>A ENSP00000512479.1:n.753+2T>A
ENST00000696197.1:c.753+2T>A ENSP00000512480.1:n.753+2T>A
ENST00000696225.1:c.753+2T>A ENSP00000512491.1:n.753+2T>A
ENST00000696226.1:c.755T>A ENSP00000512492.1:p.Val252Glu
ENST00000696227.1:c.*307T>A ENSP00000512493.1:n.*307T>A
XM_006724080.2:c.-1582+2T>A XP_006724143.1:n.-1582+2T>A
XM_006724080.3:c.-1582+2T>A XP_006724143.1:n.-1582+2T>A
XM_011546133.1:c.753+2T>A XP_011544435.1:n.753+2T>A
XM_011546133.2:c.753+2T>A XP_011544435.1:n.753+2T>A