Canonical Allele Identifier: CA354217818
Gene: ADCY5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123319714T>A , CM000665.2:g.123319714T>A GRCh38
NC_000003.11:g.123038561T>A , CM000665.1:g.123038561T>A GRCh37
NC_000003.10:g.124521251T>A NCBI36
NG_033882.1:g.133832A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.893A>T ENSP00000420082.2:p.Lys298Met
ENST00000470367.2:c.1181A>T ENSP00000514541.1:p.Lys394Met
ENST00000483566.2:c.893A>T ENSP00000420252.2:p.Lys298Met
ENST00000699714.1:c.893A>T ENSP00000514539.1:p.Lys298Met
ENST00000699715.1:c.893A>T ENSP00000514540.1:p.Lys298Met
ENST00000699716.1:c.893A>T ENSP00000514542.1:p.Lys298Met
ENST00000699718.1:c.2216A>T ENSP00000514543.1:p.Lys739Met
ENST00000699719.1:n.475A>T
ENST00000462833.6:c.2216A>T MANE Select ENSP00000419361.1:p.Lys739Met
ENST00000309879.9:c.1166A>T ENSP00000308685.5:p.Lys389Met
ENST00000462833.5:c.2216A>T ENSP00000419361.1:p.Lys739Met
ENST00000466617.5:c.893A>T ENSP00000420082.1:p.Lys298Met
ENST00000491190.5:c.1115A>T ENSP00000418537.1:p.Lys372Met
NM_001199642.1:c.1166A>T NP_001186571.1:p.Lys389Met
NM_183357.2:c.2216A>T NP_899200.1:p.Lys739Met
XM_005247077.2:c.2216A>T XP_005247134.1:p.Lys739Met
XM_005247078.1:c.1166A>T XP_005247135.1:p.Lys389Met
XM_006713483.1:c.1115A>T XP_006713546.1:p.Lys372Met
XM_006713484.1:c.893A>T XP_006713547.1:p.Lys298Met
XM_011512358.1:c.2216A>T XP_011510660.1:p.Lys739Met
XM_011512359.1:c.1217A>T XP_011510661.1:p.Lys406Met
XM_011512360.1:c.1127A>T XP_011510662.1:p.Lys376Met
XM_011512361.1:c.893A>T XP_011510663.1:p.Lys298Met
XM_005247077.4:c.2216A>T XP_005247134.1:p.Lys739Met
XM_011512359.2:c.1217A>T XP_011510661.1:p.Lys406Met
XM_011512360.3:c.1127A>T XP_011510662.1:p.Lys376Met
XM_017005638.1:c.1118A>T XP_016861127.1:p.Lys373Met
XM_017005639.1:c.1118A>T XP_016861128.1:p.Lys373Met
NM_001378259.1:c.2216A>T NP_001365188.1:p.Lys739Met
NM_183357.3:c.2216A>T MANE Select NP_899200.1:p.Lys739Met