Canonical Allele Identifier: CA4208959

Gene: ADCYAP1R1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.31078019G>A , CM000669.2:g.31078019G>A	GRCh38
NC_000007.13:g.31117634G>A , CM000669.1:g.31117634G>A	GRCh37
NC_000007.12:g.31084159G>A	NCBI36
NG_029869.1:g.30559G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001118.5:c.186G>A MANE Select	NP_001109.2:p.Thr62=
ENST00000304166.9:c.186G>A MANE Select	ENSP00000306620.4:p.Thr62=
NM_001118.4:c.186G>A	NP_001109.2:p.Thr62=
NM_001199635.1:c.186G>A	NP_001186564.1:p.Thr62=
NM_001199635.2:c.186G>A	NP_001186564.1:p.Thr62=
NM_001199636.1:c.186G>A	NP_001186565.1:p.Thr62=
NM_001199636.2:c.186G>A	NP_001186565.1:p.Thr62=
NM_001199637.1:c.186G>A	NP_001186566.1:p.Thr62=
NM_001199637.2:c.186G>A	NP_001186566.1:p.Thr62=
ENST00000304166.8:c.186G>A	ENSP00000306620.4:p.Thr62=
ENST00000396211.6:c.186G>A	ENSP00000379514.2:p.Thr62=
ENST00000396211.7:c.186G>A	ENSP00000379514.2:p.Thr62=
ENST00000409363.5:c.186G>A	ENSP00000387335.1:p.Thr62=
ENST00000409489.5:c.186G>A	ENSP00000386395.1:p.Thr62=
ENST00000431811.5:c.186G>A	ENSP00000400893.1:p.Thr62=
ENST00000614107.4:c.186G>A	ENSP00000483721.1:p.Thr62=
ENST00000705423.1:c.186G>A	ENSP00000516124.1:p.Thr62=
ENST00000705424.1:c.186G>A	ENSP00000516125.1:p.Thr62=
XM_005249618.3:c.158-6122G>A	XP_005249675.1:n.158-6122G>A
XM_005249618.5:c.158-6122G>A	XP_005249675.1:n.158-6122G>A
XM_006715645.1:c.186G>A	XP_006715708.1:p.Thr62=
XM_006715645.3:c.186G>A	XP_006715708.1:p.Thr62=
XM_011515117.1:c.186G>A	XP_011513419.1:p.Thr62=
XM_011515118.1:c.186G>A	XP_011513420.1:p.Thr62=
XM_011515119.1:c.186G>A	XP_011513421.1:p.Thr62=
XM_011515120.1:c.158-6122G>A	XP_011513422.1:n.158-6122G>A
XM_017011736.2:c.186G>A	XP_016867225.1:p.Thr62=
XM_017011737.2:c.186G>A	XP_016867226.1:p.Thr62=
XM_017011738.2:c.158-6122G>A	XP_016867227.1:n.158-6122G>A