Canonical Allele Identifier: CA499227718

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283527G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956509G>C , CM000679.2:g.30956509G>C	GRCh38
NC_000017.10:g.29283527G>C , CM000679.1:g.29283527G>C	GRCh37
NC_000017.9:g.26307653G>C	NCBI36
NG_051975.1:g.39774G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1111+40G>C MANE Select	ENSP00000329468.3:n.1111+40G>C
ENST00000330889.7:c.1111+40G>C	ENSP00000329468.3:n.1111+40G>C
ENST00000470962.1:n.531+40G>C
ENST00000480980.1:n.585G>C
ENST00000580525.5:c.1129+40G>C	ENSP00000464121.1:n.1129+40G>C
ENST00000584828.5:c.402+118G>C
ENST00000585130.5:c.*710+40G>C	ENSP00000464120.1:n.*710+40G>C
NM_018404.2:c.1111+40G>C	NP_060874.1:n.1111+40G>C
XM_005258008.2:c.1129+40G>C	XP_005258065.1:n.1129+40G>C
XM_005258011.2:c.1066+40G>C	XP_005258068.1:n.1066+40G>C
XM_006721973.2:c.1051+118G>C	XP_006722036.1:n.1051+118G>C
XM_011524993.1:c.1126+40G>C	XP_011523295.1:n.1126+40G>C
XM_011524994.1:c.1108+40G>C	XP_011523296.1:n.1108+40G>C
NM_001346712.1:c.1129+40G>C	NP_001333641.1:n.1129+40G>C
NM_001346714.1:c.1108+40G>C	NP_001333643.1:n.1108+40G>C
NM_001346716.1:c.1033+118G>C	NP_001333645.1:n.1033+118G>C
NR_144488.1:n.1310+40G>C
XM_024450831.1:c.1151G>C	XP_024306599.1:p.Gly384Ala
XM_024450832.1:c.1126+40G>C	XP_024306600.1:n.1126+40G>C
XM_024450833.1:c.1066+40G>C	XP_024306601.1:n.1066+40G>C
XM_024450834.1:c.1051+118G>C	XP_024306602.1:n.1051+118G>C
XM_024450835.1:c.745+40G>C	XP_024306603.1:n.745+40G>C
NM_018404.3:c.1111+40G>C MANE Select	NP_060874.1:n.1111+40G>C
NM_001346712.2:c.1129+40G>C	NP_001333641.1:n.1129+40G>C
NM_001346714.2:c.1108+40G>C	NP_001333643.1:n.1108+40G>C
NM_001346716.2:c.1033+118G>C	NP_001333645.1:n.1033+118G>C
NR_144488.2:n.1101+40G>C