Canonical Allele Identifier: CA398978971

Gene: ADAP2

Linked Data

• dbSNP Id: rs144212441
• gnomAD v4: 17-30956250-G-C
• MyVariant Identifiers: chr17:g.29283268G>C (hg19) ; chr17:g.30956250G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956250G>C , CM000679.2:g.30956250G>C	GRCh38
NC_000017.10:g.29283268G>C , CM000679.1:g.29283268G>C	GRCh37
NC_000017.9:g.26307394G>C	NCBI36
NG_051975.1:g.39515G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.892G>C MANE Select	ENSP00000329468.3:p.Glu298Gln
ENST00000330889.7:c.892G>C	ENSP00000329468.3:p.Glu298Gln
ENST00000470962.1:n.312G>C
ENST00000480980.1:n.326G>C
ENST00000580525.5:c.910G>C	ENSP00000464121.1:p.Glu304Gln
ENST00000581285.5:c.808G>C	ENSP00000464155.1:p.Glu270Gln
ENST00000584828.5:c.261G>C
ENST00000584989.1:c.184G>C	ENSP00000462634.1:p.Glu62Gln
ENST00000585130.5:c.*491G>C	ENSP00000464120.1:n.*491G>C
NM_018404.2:c.892G>C	NP_060874.1:p.Glu298Gln
XM_005258008.2:c.910G>C	XP_005258065.1:p.Glu304Gln
XM_005258011.2:c.847G>C	XP_005258068.1:p.Glu283Gln
XM_006721973.2:c.910G>C	XP_006722036.1:p.Glu304Gln
XM_011524993.1:c.907G>C	XP_011523295.1:p.Glu303Gln
XM_011524994.1:c.889G>C	XP_011523296.1:p.Glu297Gln
NM_001346712.1:c.910G>C	NP_001333641.1:p.Glu304Gln
NM_001346714.1:c.889G>C	NP_001333643.1:p.Glu297Gln
NM_001346716.1:c.892G>C	NP_001333645.1:p.Glu298Gln
NR_144488.1:n.1091G>C
XM_024450831.1:c.892G>C	XP_024306599.1:p.Glu298Gln
XM_024450832.1:c.907G>C	XP_024306600.1:p.Glu303Gln
XM_024450833.1:c.847G>C	XP_024306601.1:p.Glu283Gln
XM_024450834.1:c.910G>C	XP_024306602.1:p.Glu304Gln
XM_024450835.1:c.526G>C	XP_024306603.1:p.Glu176Gln
NM_018404.3:c.892G>C MANE Select	NP_060874.1:p.Glu298Gln
NM_001346712.2:c.910G>C	NP_001333641.1:p.Glu304Gln
NM_001346714.2:c.889G>C	NP_001333643.1:p.Glu297Gln
NM_001346716.2:c.892G>C	NP_001333645.1:p.Glu298Gln
NR_144488.2:n.882G>C