Canonical Allele Identifier: CA2519265323

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291367_123291368insGCCCGTCGC , CM000665.2:g.123291367_123291368insGCCCGTCGC	GRCh38
NC_000003.11:g.123010214_123010215insGCCCGTCGC , CM000665.1:g.123010214_123010215insGCCCGTCGC	GRCh37
NC_000003.10:g.124492904_124492905insGCCCGTCGC	NCBI36
NG_033882.1:g.162179_162180insCGACGGGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000466617.6:c.1750_1751insCGACGGGCG	ENSP00000420082.2:p.Glu583_Glu584insAlaTh...
ENST00000470367.2:c.2038_2039insCGACGGGCG	ENSP00000514541.1:p.Glu679_Glu680insAlaTh...
ENST00000483566.2:c.1750_1751insCGACGGGCG	ENSP00000420252.2:p.Glu583_Glu584insAlaTh...
ENST00000699714.1:c.1750_1751insCGACGGGCG	ENSP00000514539.1:p.Glu583_Glu584insAlaTh...
ENST00000699715.1:c.1750_1751insCGACGGGCG	ENSP00000514540.1:p.Glu583_Glu584insAlaTh...
ENST00000699716.1:c.1750_1751insCGACGGGCG	ENSP00000514542.1:p.Glu583_Glu584insAlaTh...
ENST00000699717.1:n.1476_1477insCGACGGGCG
ENST00000699718.1:c.3148_3149insCGACGGGCG	ENSP00000514543.1:p.Glu1049_Glu1050insAla...
ENST00000462833.6:c.3073_3074insCGACGGGCG MANE Select	ENSP00000419361.1:p.Glu1024_Glu1025insAla...
ENST00000309879.9:c.2023_2024insCGACGGGCG	ENSP00000308685.5:p.Glu674_Glu675insAlaTh...
ENST00000462833.5:c.3073_3074insCGACGGGCG	ENSP00000419361.1:p.Glu1024_Glu1025insAla...
ENST00000491190.5:c.2047_2048insCGACGGGCG	ENSP00000418537.1:p.Glu682_Glu683insAlaTh...
NM_001199642.1:c.2023_2024insCGACGGGCG	NP_001186571.1:p.Glu674_Glu675insAlaThrGl...
NM_183357.2:c.3073_3074insCGACGGGCG	NP_899200.1:p.Glu1024_Glu1025insAlaThrGly...
XM_005247077.2:c.3148_3149insCGACGGGCG	XP_005247134.1:p.Glu1049_Glu1050insAlaThr...
XM_005247078.1:c.2098_2099insCGACGGGCG	XP_005247135.1:p.Glu699_Glu700insAlaThrGl...
XM_006713483.1:c.2047_2048insCGACGGGCG	XP_006713546.1:p.Glu682_Glu683insAlaThrGl...
XM_006713484.1:c.1825_1826insCGACGGGCG	XP_006713547.1:p.Glu608_Glu609insAlaThrGl...
XM_011512359.1:c.2149_2150insCGACGGGCG	XP_011510661.1:p.Glu716_Glu717insAlaThrGl...
XM_011512360.1:c.2059_2060insCGACGGGCG	XP_011510662.1:p.Glu686_Glu687insAlaThrGl...
XM_011512361.1:c.1825_1826insCGACGGGCG	XP_011510663.1:p.Glu608_Glu609insAlaThrGl...
XM_005247077.4:c.3148_3149insCGACGGGCG	XP_005247134.1:p.Glu1049_Glu1050insAlaThr...
XM_011512359.2:c.2149_2150insCGACGGGCG	XP_011510661.1:p.Glu716_Glu717insAlaThrGl...
XM_011512360.3:c.2059_2060insCGACGGGCG	XP_011510662.1:p.Glu686_Glu687insAlaThrGl...
XM_017005638.1:c.2050_2051insCGACGGGCG	XP_016861127.1:p.Glu683_Glu684insAlaThrGl...
XM_017005639.1:c.2050_2051insCGACGGGCG	XP_016861128.1:p.Glu683_Glu684insAlaThrGl...
NM_001378259.1:c.3148_3149insCGACGGGCG	NP_001365188.1:p.Glu1049_Glu1050insAlaThr...
NM_183357.3:c.3073_3074insCGACGGGCG MANE Select	NP_899200.1:p.Glu1024_Glu1025insAlaThrGly...