Canonical Allele Identifier: CA398979027

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283293A>C (hg19) ; chr17:g.30956275A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956275A>C , CM000679.2:g.30956275A>C	GRCh38
NC_000017.10:g.29283293A>C , CM000679.1:g.29283293A>C	GRCh37
NC_000017.9:g.26307419A>C	NCBI36
NG_051975.1:g.39540A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.917A>C MANE Select	ENSP00000329468.3:p.Asn306Thr
ENST00000330889.7:c.917A>C	ENSP00000329468.3:p.Asn306Thr
ENST00000470962.1:n.337A>C
ENST00000480980.1:n.351A>C
ENST00000580525.5:c.935A>C	ENSP00000464121.1:p.Asn312Thr
ENST00000581285.5:c.833A>C	ENSP00000464155.1:p.Asn278Thr
ENST00000584828.5:c.286A>C
ENST00000584989.1:c.209A>C	ENSP00000462634.1:p.Asn70Thr
ENST00000585130.5:c.*516A>C	ENSP00000464120.1:n.*516A>C
NM_018404.2:c.917A>C	NP_060874.1:p.Asn306Thr
XM_005258008.2:c.935A>C	XP_005258065.1:p.Asn312Thr
XM_005258011.2:c.872A>C	XP_005258068.1:p.Asn291Thr
XM_006721973.2:c.935A>C	XP_006722036.1:p.Asn312Thr
XM_011524993.1:c.932A>C	XP_011523295.1:p.Asn311Thr
XM_011524994.1:c.914A>C	XP_011523296.1:p.Asn305Thr
NM_001346712.1:c.935A>C	NP_001333641.1:p.Asn312Thr
NM_001346714.1:c.914A>C	NP_001333643.1:p.Asn305Thr
NM_001346716.1:c.917A>C	NP_001333645.1:p.Asn306Thr
NR_144488.1:n.1116A>C
XM_024450831.1:c.917A>C	XP_024306599.1:p.Asn306Thr
XM_024450832.1:c.932A>C	XP_024306600.1:p.Asn311Thr
XM_024450833.1:c.872A>C	XP_024306601.1:p.Asn291Thr
XM_024450834.1:c.935A>C	XP_024306602.1:p.Asn312Thr
XM_024450835.1:c.551A>C	XP_024306603.1:p.Asn184Thr
NM_018404.3:c.917A>C MANE Select	NP_060874.1:p.Asn306Thr
NM_001346712.2:c.935A>C	NP_001333641.1:p.Asn312Thr
NM_001346714.2:c.914A>C	NP_001333643.1:p.Asn305Thr
NM_001346716.2:c.917A>C	NP_001333645.1:p.Asn306Thr
NR_144488.2:n.907A>C