Canonical Allele Identifier: CA114173098
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs3073883

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7650245_7650248dup , CM000667.2:g.7650245_7650248dup GRCh38
NC_000005.9:g.7650358_7650361dup , CM000667.1:g.7650358_7650361dup GRCh37
NC_000005.8:g.7703358_7703361dup NCBI36
NG_046913.1:g.259016_259019dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338316.9:c.720+23929_720+23932dup MANE Select ENSP00000342952.4:n.720+23929_720+23932dup
ENST00000338316.8:c.720+23929_720+23932dup ENSP00000342952.4:n.720+23929_720+23932dup
ENST00000498598.1:n.420-7781_420-7778dup
ENST00000515681.1:c.87+23929_87+23932dup ENSP00000425069.1:n.87+23929_87+23932dup
ENST00000537121.5:c.714+23929_714+23932dup ENSP00000444803.2:n.714+23929_714+23932dup
NM_020546.2:c.720+23929_720+23932dup NP_065433.2:n.720+23929_720+23932dup
XM_011513942.1:c.720+23929_720+23932dup XP_011512244.1:n.720+23929_720+23932dup
XR_427657.2:n.734+23929_734+23932dup
XM_011513942.2:c.720+23929_720+23932dup XP_011512244.1:n.720+23929_720+23932dup
XR_001741973.1:n.734+23929_734+23932dup
XR_001741974.2:n.734+23929_734+23932dup
NM_020546.3:c.720+23929_720+23932dup MANE Select NP_065433.2:n.720+23929_720+23932dup