Canonical Allele Identifier: CA1525691555
Gene: ADCY2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7617115_7617119delinsTCCCA , CM000667.2:g.7617115_7617119delinsTCCCA GRCh38
NC_000005.9:g.7617228_7617232delinsTCCCA , CM000667.1:g.7617228_7617232delinsTCCCA GRCh37
NC_000005.8:g.7670228_7670232delinsTCCCA NCBI36
NG_046913.1:g.225886_225890delinsTCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338316.9:c.571-9052_571-9048delinsTCCCA MANE Select ENSP00000342952.4:n.571-9052_571-9048delinsTCCCA
ENST00000338316.8:c.571-9052_571-9048delinsTCCCA ENSP00000342952.4:n.571-9052_571-9048delinsTCCCA
ENST00000498598.1:n.270-9052_270-9048delinsTCCCA
ENST00000515681.1:c.-64+5940_-64+5944delinsTCCCA ENSP00000425069.1:n.-64+5940_-64+5944delinsTCCCA
ENST00000537121.5:c.566-9052_566-9048delinsTCCCA ENSP00000444803.2:n.566-9052_566-9048delinsTCCCA
NM_020546.2:c.571-9052_571-9048delinsTCCCA NP_065433.2:n.571-9052_571-9048delinsTCCCA
XM_011513942.1:c.571-9052_571-9048delinsTCCCA XP_011512244.1:n.571-9052_571-9048delinsTCCCA
XR_427657.2:n.585-9052_585-9048delinsTCCCA
XM_011513942.2:c.571-9052_571-9048delinsTCCCA XP_011512244.1:n.571-9052_571-9048delinsTCCCA
XR_001741973.1:n.585-9052_585-9048delinsTCCCA
XR_001741974.2:n.585-9052_585-9048delinsTCCCA
NM_020546.3:c.571-9052_571-9048delinsTCCCA MANE Select NP_065433.2:n.571-9052_571-9048delinsTCCCA