Canonical Allele Identifier: CA398978960

Gene: ADAP2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.886G>C MANE Select	ENSP00000329468.3:p.Ala296Pro
ENST00000330889.7:c.886G>C	ENSP00000329468.3:p.Ala296Pro
ENST00000470962.1:n.306G>C
ENST00000480980.1:n.320G>C
ENST00000580525.5:c.904G>C	ENSP00000464121.1:p.Ala302Pro
ENST00000581285.5:c.802G>C	ENSP00000464155.1:p.Ala268Pro
ENST00000584828.5:c.255G>C
ENST00000584989.1:c.178G>C	ENSP00000462634.1:p.Ala60Pro
ENST00000585130.5:c.*485G>C	ENSP00000464120.1:n.*485G>C
NM_018404.2:c.886G>C	NP_060874.1:p.Ala296Pro
XM_005258008.2:c.904G>C	XP_005258065.1:p.Ala302Pro
XM_005258011.2:c.841G>C	XP_005258068.1:p.Ala281Pro
XM_006721973.2:c.904G>C	XP_006722036.1:p.Ala302Pro
XM_011524993.1:c.901G>C	XP_011523295.1:p.Ala301Pro
XM_011524994.1:c.883G>C	XP_011523296.1:p.Ala295Pro
NM_001346712.1:c.904G>C	NP_001333641.1:p.Ala302Pro
NM_001346714.1:c.883G>C	NP_001333643.1:p.Ala295Pro
NM_001346716.1:c.886G>C	NP_001333645.1:p.Ala296Pro
NR_144488.1:n.1085G>C
XM_024450831.1:c.886G>C	XP_024306599.1:p.Ala296Pro
XM_024450832.1:c.901G>C	XP_024306600.1:p.Ala301Pro
XM_024450833.1:c.841G>C	XP_024306601.1:p.Ala281Pro
XM_024450834.1:c.904G>C	XP_024306602.1:p.Ala302Pro
XM_024450835.1:c.520G>C	XP_024306603.1:p.Ala174Pro
NM_018404.3:c.886G>C MANE Select	NP_060874.1:p.Ala296Pro
NM_001346712.2:c.904G>C	NP_001333641.1:p.Ala302Pro
NM_001346714.2:c.883G>C	NP_001333643.1:p.Ala295Pro
NM_001346716.2:c.886G>C	NP_001333645.1:p.Ala296Pro
NR_144488.2:n.876G>C