Canonical Allele Identifier: CA367149953
Gene: ADCYAP1R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.31085329A>G , CM000669.2:g.31085329A>G GRCh38
NC_000007.13:g.31124944A>G , CM000669.1:g.31124944A>G GRCh37
NC_000007.12:g.31091469A>G NCBI36
NG_029869.1:g.37869A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396211.7:c.556A>G ENSP00000379514.2:p.Asn186Asp
ENST00000705423.1:c.556A>G ENSP00000516124.1:p.Asn186Asp
ENST00000705424.1:c.556A>G ENSP00000516125.1:p.Asn186Asp
ENST00000304166.9:c.556A>G MANE Select ENSP00000306620.4:p.Asn186Asp
ENST00000304166.8:c.556A>G ENSP00000306620.4:p.Asn186Asp
ENST00000396211.6:c.556A>G ENSP00000379514.2:p.Asn186Asp
ENST00000409363.5:c.493A>G ENSP00000387335.1:p.Asn165Asp
ENST00000409489.5:c.556A>G ENSP00000386395.1:p.Asn186Asp
ENST00000614107.4:c.556A>G ENSP00000483721.1:p.Asn186Asp
NM_001118.4:c.556A>G NP_001109.2:p.Asn186Asp
NM_001199635.1:c.556A>G NP_001186564.1:p.Asn186Asp
NM_001199636.1:c.556A>G NP_001186565.1:p.Asn186Asp
NM_001199637.1:c.493A>G NP_001186566.1:p.Asn165Asp
XM_005249618.3:c.385A>G XP_005249675.1:p.Asn129Asp
XM_006715645.1:c.556A>G XP_006715708.1:p.Asn186Asp
XM_011515117.1:c.556A>G XP_011513419.1:p.Asn186Asp
XM_011515118.1:c.535A>G XP_011513420.1:p.Asn179Asp
XM_011515119.1:c.493A>G XP_011513421.1:p.Asn165Asp
XM_011515120.1:c.385A>G XP_011513422.1:p.Asn129Asp
XM_005249618.5:c.385A>G XP_005249675.1:p.Asn129Asp
XM_006715645.3:c.556A>G XP_006715708.1:p.Asn186Asp
XM_017011736.2:c.535A>G XP_016867225.1:p.Asn179Asp
XM_017011737.2:c.493A>G XP_016867226.1:p.Asn165Asp
XM_017011738.2:c.385A>G XP_016867227.1:p.Asn129Asp
NM_001118.5:c.556A>G MANE Select NP_001109.2:p.Asn186Asp
NM_001199636.2:c.556A>G NP_001186565.1:p.Asn186Asp
NM_001199637.2:c.493A>G NP_001186566.1:p.Asn165Asp
NM_001199635.2:c.556A>G NP_001186564.1:p.Asn186Asp