Canonical Allele Identifier: CA4209382

Gene: ADCYAP1R1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.31106574C>G , CM000669.2:g.31106574C>G	GRCh38
NC_000007.13:g.31146188C>G , CM000669.1:g.31146188C>G	GRCh37
NC_000007.12:g.31112713C>G	NCBI36
NG_029869.1:g.59113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396211.7:c.1381C>G	ENSP00000379514.2:p.Pro461Ala
ENST00000705423.1:c.1378C>G	ENSP00000516124.1:p.Pro460Ala
ENST00000705424.1:c.1381C>G	ENSP00000516125.1:p.Pro461Ala
ENST00000304166.9:c.1297C>G MANE Select	ENSP00000306620.4:p.Pro433Ala
ENST00000304166.8:c.1297C>G	ENSP00000306620.4:p.Pro433Ala
ENST00000396211.6:c.1381C>G	ENSP00000379514.2:p.Pro461Ala
ENST00000409363.5:c.1234C>G	ENSP00000387335.1:p.Pro412Ala
ENST00000409489.5:c.1465C>G	ENSP00000386395.1:p.Pro489Ala
ENST00000614107.4:c.1381C>G	ENSP00000483721.1:p.Pro461Ala
NM_001118.4:c.1297C>G	NP_001109.2:p.Pro433Ala
NM_001199635.1:c.1381C>G	NP_001186564.1:p.Pro461Ala
NM_001199636.1:c.1378C>G	NP_001186565.1:p.Pro460Ala
NM_001199637.1:c.1234C>G	NP_001186566.1:p.Pro412Ala
XM_005249618.3:c.1126C>G	XP_005249675.1:p.Pro376Ala
XM_006715645.1:c.1381C>G	XP_006715708.1:p.Pro461Ala
XM_011515117.1:c.1462C>G	XP_011513419.1:p.Pro488Ala
XM_011515118.1:c.1441C>G	XP_011513420.1:p.Pro481Ala
XM_011515119.1:c.1399C>G	XP_011513421.1:p.Pro467Ala
XM_011515120.1:c.1291C>G	XP_011513422.1:p.Pro431Ala
XM_005249618.5:c.1126C>G	XP_005249675.1:p.Pro376Ala
XM_006715645.3:c.1381C>G	XP_006715708.1:p.Pro461Ala
XM_017011736.2:c.1360C>G	XP_016867225.1:p.Pro454Ala
XM_017011737.2:c.1318C>G	XP_016867226.1:p.Pro440Ala
XM_017011738.2:c.1210C>G	XP_016867227.1:p.Pro404Ala
NM_001118.5:c.1297C>G MANE Select	NP_001109.2:p.Pro433Ala
NM_001199636.2:c.1378C>G	NP_001186565.1:p.Pro460Ala
NM_001199637.2:c.1234C>G	NP_001186566.1:p.Pro412Ala
NM_001199635.2:c.1381C>G	NP_001186564.1:p.Pro461Ala