Canonical Allele Identifier: CA398978995

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283278A>C (hg19) ; chr17:g.30956260A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956260A>C , CM000679.2:g.30956260A>C	GRCh38
NC_000017.10:g.29283278A>C , CM000679.1:g.29283278A>C	GRCh37
NC_000017.9:g.26307404A>C	NCBI36
NG_051975.1:g.39525A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.902A>C MANE Select	ENSP00000329468.3:p.Gln301Pro
ENST00000330889.7:c.902A>C	ENSP00000329468.3:p.Gln301Pro
ENST00000470962.1:n.322A>C
ENST00000480980.1:n.336A>C
ENST00000580525.5:c.920A>C	ENSP00000464121.1:p.Gln307Pro
ENST00000581285.5:c.818A>C	ENSP00000464155.1:p.Gln273Pro
ENST00000584828.5:c.271A>C
ENST00000584989.1:c.194A>C	ENSP00000462634.1:p.Gln65Pro
ENST00000585130.5:c.*501A>C	ENSP00000464120.1:n.*501A>C
NM_018404.2:c.902A>C	NP_060874.1:p.Gln301Pro
XM_005258008.2:c.920A>C	XP_005258065.1:p.Gln307Pro
XM_005258011.2:c.857A>C	XP_005258068.1:p.Gln286Pro
XM_006721973.2:c.920A>C	XP_006722036.1:p.Gln307Pro
XM_011524993.1:c.917A>C	XP_011523295.1:p.Gln306Pro
XM_011524994.1:c.899A>C	XP_011523296.1:p.Gln300Pro
NM_001346712.1:c.920A>C	NP_001333641.1:p.Gln307Pro
NM_001346714.1:c.899A>C	NP_001333643.1:p.Gln300Pro
NM_001346716.1:c.902A>C	NP_001333645.1:p.Gln301Pro
NR_144488.1:n.1101A>C
XM_024450831.1:c.902A>C	XP_024306599.1:p.Gln301Pro
XM_024450832.1:c.917A>C	XP_024306600.1:p.Gln306Pro
XM_024450833.1:c.857A>C	XP_024306601.1:p.Gln286Pro
XM_024450834.1:c.920A>C	XP_024306602.1:p.Gln307Pro
XM_024450835.1:c.536A>C	XP_024306603.1:p.Gln179Pro
NM_018404.3:c.902A>C MANE Select	NP_060874.1:p.Gln301Pro
NM_001346712.2:c.920A>C	NP_001333641.1:p.Gln307Pro
NM_001346714.2:c.899A>C	NP_001333643.1:p.Gln300Pro
NM_001346716.2:c.902A>C	NP_001333645.1:p.Gln301Pro
NR_144488.2:n.892A>C