Canonical Allele Identifier: CA398978959

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283262G>A (hg19) ; chr17:g.30956244G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956244G>A , CM000679.2:g.30956244G>A	GRCh38
NC_000017.10:g.29283262G>A , CM000679.1:g.29283262G>A	GRCh37
NC_000017.9:g.26307388G>A	NCBI36
NG_051975.1:g.39509G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.886G>A MANE Select	ENSP00000329468.3:p.Ala296Thr
ENST00000330889.7:c.886G>A	ENSP00000329468.3:p.Ala296Thr
ENST00000470962.1:n.306G>A
ENST00000480980.1:n.320G>A
ENST00000580525.5:c.904G>A	ENSP00000464121.1:p.Ala302Thr
ENST00000581285.5:c.802G>A	ENSP00000464155.1:p.Ala268Thr
ENST00000584828.5:c.255G>A
ENST00000584989.1:c.178G>A	ENSP00000462634.1:p.Ala60Thr
ENST00000585130.5:c.*485G>A	ENSP00000464120.1:n.*485G>A
NM_018404.2:c.886G>A	NP_060874.1:p.Ala296Thr
XM_005258008.2:c.904G>A	XP_005258065.1:p.Ala302Thr
XM_005258011.2:c.841G>A	XP_005258068.1:p.Ala281Thr
XM_006721973.2:c.904G>A	XP_006722036.1:p.Ala302Thr
XM_011524993.1:c.901G>A	XP_011523295.1:p.Ala301Thr
XM_011524994.1:c.883G>A	XP_011523296.1:p.Ala295Thr
NM_001346712.1:c.904G>A	NP_001333641.1:p.Ala302Thr
NM_001346714.1:c.883G>A	NP_001333643.1:p.Ala295Thr
NM_001346716.1:c.886G>A	NP_001333645.1:p.Ala296Thr
NR_144488.1:n.1085G>A
XM_024450831.1:c.886G>A	XP_024306599.1:p.Ala296Thr
XM_024450832.1:c.901G>A	XP_024306600.1:p.Ala301Thr
XM_024450833.1:c.841G>A	XP_024306601.1:p.Ala281Thr
XM_024450834.1:c.904G>A	XP_024306602.1:p.Ala302Thr
XM_024450835.1:c.520G>A	XP_024306603.1:p.Ala174Thr
NM_018404.3:c.886G>A MANE Select	NP_060874.1:p.Ala296Thr
NM_001346712.2:c.904G>A	NP_001333641.1:p.Ala302Thr
NM_001346714.2:c.883G>A	NP_001333643.1:p.Ala295Thr
NM_001346716.2:c.886G>A	NP_001333645.1:p.Ala296Thr
NR_144488.2:n.876G>A