Canonical Allele Identifier: CA398978982

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283272A>T (hg19) ; chr17:g.30956254A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956254A>T , CM000679.2:g.30956254A>T	GRCh38
NC_000017.10:g.29283272A>T , CM000679.1:g.29283272A>T	GRCh37
NC_000017.9:g.26307398A>T	NCBI36
NG_051975.1:g.39519A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.896A>T MANE Select	ENSP00000329468.3:p.Gln299Leu
ENST00000330889.7:c.896A>T	ENSP00000329468.3:p.Gln299Leu
ENST00000470962.1:n.316A>T
ENST00000480980.1:n.330A>T
ENST00000580525.5:c.914A>T	ENSP00000464121.1:p.Gln305Leu
ENST00000581285.5:c.812A>T	ENSP00000464155.1:p.Gln271Leu
ENST00000584828.5:c.265A>T
ENST00000584989.1:c.188A>T	ENSP00000462634.1:p.Gln63Leu
ENST00000585130.5:c.*495A>T	ENSP00000464120.1:n.*495A>T
NM_018404.2:c.896A>T	NP_060874.1:p.Gln299Leu
XM_005258008.2:c.914A>T	XP_005258065.1:p.Gln305Leu
XM_005258011.2:c.851A>T	XP_005258068.1:p.Gln284Leu
XM_006721973.2:c.914A>T	XP_006722036.1:p.Gln305Leu
XM_011524993.1:c.911A>T	XP_011523295.1:p.Gln304Leu
XM_011524994.1:c.893A>T	XP_011523296.1:p.Gln298Leu
NM_001346712.1:c.914A>T	NP_001333641.1:p.Gln305Leu
NM_001346714.1:c.893A>T	NP_001333643.1:p.Gln298Leu
NM_001346716.1:c.896A>T	NP_001333645.1:p.Gln299Leu
NR_144488.1:n.1095A>T
XM_024450831.1:c.896A>T	XP_024306599.1:p.Gln299Leu
XM_024450832.1:c.911A>T	XP_024306600.1:p.Gln304Leu
XM_024450833.1:c.851A>T	XP_024306601.1:p.Gln284Leu
XM_024450834.1:c.914A>T	XP_024306602.1:p.Gln305Leu
XM_024450835.1:c.530A>T	XP_024306603.1:p.Gln177Leu
NM_018404.3:c.896A>T MANE Select	NP_060874.1:p.Gln299Leu
NM_001346712.2:c.914A>T	NP_001333641.1:p.Gln305Leu
NM_001346714.2:c.893A>T	NP_001333643.1:p.Gln298Leu
NM_001346716.2:c.896A>T	NP_001333645.1:p.Gln299Leu
NR_144488.2:n.886A>T