Canonical Allele Identifier: CA398978978

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283271C>A (hg19) ; chr17:g.30956253C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956253C>A , CM000679.2:g.30956253C>A	GRCh38
NC_000017.10:g.29283271C>A , CM000679.1:g.29283271C>A	GRCh37
NC_000017.9:g.26307397C>A	NCBI36
NG_051975.1:g.39518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.895C>A MANE Select	ENSP00000329468.3:p.Gln299Lys
ENST00000330889.7:c.895C>A	ENSP00000329468.3:p.Gln299Lys
ENST00000470962.1:n.315C>A
ENST00000480980.1:n.329C>A
ENST00000580525.5:c.913C>A	ENSP00000464121.1:p.Gln305Lys
ENST00000581285.5:c.811C>A	ENSP00000464155.1:p.Gln271Lys
ENST00000584828.5:c.264C>A
ENST00000584989.1:c.187C>A	ENSP00000462634.1:p.Gln63Lys
ENST00000585130.5:c.*494C>A	ENSP00000464120.1:n.*494C>A
NM_018404.2:c.895C>A	NP_060874.1:p.Gln299Lys
XM_005258008.2:c.913C>A	XP_005258065.1:p.Gln305Lys
XM_005258011.2:c.850C>A	XP_005258068.1:p.Gln284Lys
XM_006721973.2:c.913C>A	XP_006722036.1:p.Gln305Lys
XM_011524993.1:c.910C>A	XP_011523295.1:p.Gln304Lys
XM_011524994.1:c.892C>A	XP_011523296.1:p.Gln298Lys
NM_001346712.1:c.913C>A	NP_001333641.1:p.Gln305Lys
NM_001346714.1:c.892C>A	NP_001333643.1:p.Gln298Lys
NM_001346716.1:c.895C>A	NP_001333645.1:p.Gln299Lys
NR_144488.1:n.1094C>A
XM_024450831.1:c.895C>A	XP_024306599.1:p.Gln299Lys
XM_024450832.1:c.910C>A	XP_024306600.1:p.Gln304Lys
XM_024450833.1:c.850C>A	XP_024306601.1:p.Gln284Lys
XM_024450834.1:c.913C>A	XP_024306602.1:p.Gln305Lys
XM_024450835.1:c.529C>A	XP_024306603.1:p.Gln177Lys
NM_018404.3:c.895C>A MANE Select	NP_060874.1:p.Gln299Lys
NM_001346712.2:c.913C>A	NP_001333641.1:p.Gln305Lys
NM_001346714.2:c.892C>A	NP_001333643.1:p.Gln298Lys
NM_001346716.2:c.895C>A	NP_001333645.1:p.Gln299Lys
NR_144488.2:n.885C>A