Canonical Allele Identifier: CA410233739

Gene: ADA2

Linked Data

• MyVariant Identifiers: chr22:g.17670877C>A (hg19) ; chr22:g.17189987C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17189987C>A , CM000684.2:g.17189987C>A	GRCh38
NC_000022.10:g.17670877C>A , CM000684.1:g.17670877C>A	GRCh37
NC_000022.9:g.16050877C>A	NCBI36
NG_033943.1:g.36868G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330232.9:c.204G>T	ENSP00000332871.4:p.Met68Ile
ENST00000449907.8:c.801G>T	ENSP00000406443.2:p.Met267Ile
ENST00000543038.2:c.927G>T	ENSP00000442482.2:p.Met309Ile
ENST00000610390.5:c.567G>T	ENSP00000483418.1:p.Met189Ile
ENST00000648061.2:c.159-1540G>T	ENSP00000496894.1:n.159-1540G>T
ENST00000649310.2:c.927G>T	ENSP00000496839.2:p.Met309Ile
ENST00000649746.2:c.927G>T	ENSP00000497913.2:p.Met309Ile
ENST00000649915.2:c.*2049G>T	ENSP00000497681.2:n.*2049G>T
ENST00000696189.1:n.228G>T
ENST00000696196.1:c.927G>T	ENSP00000512479.1:p.Met309Ile
ENST00000696197.1:c.927G>T	ENSP00000512480.1:p.Met309Ile
ENST00000696220.1:c.174G>T	ENSP00000512486.1:p.Met58Ile
ENST00000696221.1:c.174G>T	ENSP00000512487.1:p.Met58Ile
ENST00000696222.1:c.174G>T	ENSP00000512488.1:p.Met58Ile
ENST00000696223.1:c.174G>T	ENSP00000512489.1:p.Met58Ile
ENST00000696224.1:c.321G>T	ENSP00000512490.1:p.Met107Ile
ENST00000696225.1:c.927G>T	ENSP00000512491.1:p.Met309Ile
ENST00000399837.8:c.927G>T MANE Select	ENSP00000382731.2:p.Met309Ile
ENST00000449907.7:c.801G>T	ENSP00000406443.2:p.Met267Ile
ENST00000648061.1:c.159-1540G>T	ENSP00000496894.1:n.159-1540G>T
ENST00000648668.1:n.365G>T
ENST00000649540.1:c.801G>T	ENSP00000497469.1:p.Met267Ile
ENST00000649915.1:c.2440G>T
ENST00000262607.3:c.927G>T	ENSP00000262607.2:p.Met309Ile
ENST00000330232.8:c.204G>T	ENSP00000332871.4:p.Met68Ile
ENST00000399837.6:c.927G>T	ENSP00000382731.2:p.Met309Ile
ENST00000399839.5:c.927G>T	ENSP00000382733.1:p.Met309Ile
ENST00000449907.6:c.801G>T	ENSP00000406443.2:p.Met267Ile
ENST00000480276.1:n.367G>T
ENST00000610390.4:c.567G>T	ENSP00000483418.1:p.Met189Ile
NM_001282225.1:c.927G>T	NP_001269154.1:p.Met309Ile
NM_001282226.1:c.927G>T	NP_001269155.1:p.Met309Ile
NM_001282227.1:c.801G>T	NP_001269156.1:p.Met267Ile
NM_001282228.1:c.801G>T	NP_001269157.1:p.Met267Ile
NM_001282229.1:c.567G>T	NP_001269158.1:p.Met189Ile
NM_177405.2:c.204G>T	NP_803124.1:p.Met68Ile
XM_006724080.2:c.243G>T	XP_006724143.1:p.Met81Ile
XM_011546133.1:c.927G>T	XP_011544435.1:p.Met309Ile
NM_001282225.2:c.927G>T MANE Select	NP_001269154.1:p.Met309Ile
XM_006724080.3:c.243G>T	XP_006724143.1:p.Met81Ile
XM_011546133.2:c.927G>T	XP_011544435.1:p.Met309Ile
NM_001282226.2:c.927G>T	NP_001269155.1:p.Met309Ile
NM_001282227.2:c.801G>T	NP_001269156.1:p.Met267Ile
NM_001282228.2:c.801G>T	NP_001269157.1:p.Met267Ile
NM_177405.3:c.204G>T	NP_803124.1:p.Met68Ile
NM_001282229.2:c.567G>T	NP_001269158.1:p.Met189Ile