Canonical Allele Identifier: CA1398330497

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291453_123291454delinsTG , CM000665.2:g.123291453_123291454delinsTG	GRCh38
NC_000003.11:g.123010300_123010301delinsTG , CM000665.1:g.123010300_123010301delinsTG	GRCh37
NC_000003.10:g.124492990_124492991delinsTG	NCBI36
NG_033882.1:g.162092_162093delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1741-78_1741-77delinsCA	ENSP00000420082.2:n.1741-78_1741-77delinsCA
ENST00000470367.2:c.2029-78_2029-77delinsCA	ENSP00000514541.1:n.2029-78_2029-77delinsCA
ENST00000483566.2:c.1741-78_1741-77delinsCA	ENSP00000420252.2:n.1741-78_1741-77delinsCA
ENST00000699714.1:c.1741-78_1741-77delinsCA	ENSP00000514539.1:n.1741-78_1741-77delinsCA
ENST00000699715.1:c.1741-78_1741-77delinsCA	ENSP00000514540.1:n.1741-78_1741-77delinsCA
ENST00000699716.1:c.1741-78_1741-77delinsCA	ENSP00000514542.1:n.1741-78_1741-77delinsCA
ENST00000699717.1:n.1467-78_1467-77delinsCA
ENST00000699718.1:c.3139-78_3139-77delinsCA	ENSP00000514543.1:n.3139-78_3139-77delinsCA
ENST00000462833.6:c.3064-78_3064-77delinsCA MANE Select	ENSP00000419361.1:n.3064-78_3064-77delinsCA
ENST00000309879.9:c.2014-78_2014-77delinsCA	ENSP00000308685.5:n.2014-78_2014-77delinsCA
ENST00000462833.5:c.3064-78_3064-77delinsCA	ENSP00000419361.1:n.3064-78_3064-77delinsCA
ENST00000491190.5:c.2038-78_2038-77delinsCA	ENSP00000418537.1:n.2038-78_2038-77delinsCA
NM_001199642.1:c.2014-78_2014-77delinsCA	NP_001186571.1:n.2014-78_2014-77delinsCA
NM_183357.2:c.3064-78_3064-77delinsCA	NP_899200.1:n.3064-78_3064-77delinsCA
XM_005247077.2:c.3139-78_3139-77delinsCA	XP_005247134.1:n.3139-78_3139-77delinsCA
XM_005247078.1:c.2089-78_2089-77delinsCA	XP_005247135.1:n.2089-78_2089-77delinsCA
XM_006713483.1:c.2038-78_2038-77delinsCA	XP_006713546.1:n.2038-78_2038-77delinsCA
XM_006713484.1:c.1816-78_1816-77delinsCA	XP_006713547.1:n.1816-78_1816-77delinsCA
XM_011512359.1:c.2140-78_2140-77delinsCA	XP_011510661.1:n.2140-78_2140-77delinsCA
XM_011512360.1:c.2050-78_2050-77delinsCA	XP_011510662.1:n.2050-78_2050-77delinsCA
XM_011512361.1:c.1816-78_1816-77delinsCA	XP_011510663.1:n.1816-78_1816-77delinsCA
XM_005247077.4:c.3139-78_3139-77delinsCA	XP_005247134.1:n.3139-78_3139-77delinsCA
XM_011512359.2:c.2140-78_2140-77delinsCA	XP_011510661.1:n.2140-78_2140-77delinsCA
XM_011512360.3:c.2050-78_2050-77delinsCA	XP_011510662.1:n.2050-78_2050-77delinsCA
XM_017005638.1:c.2041-78_2041-77delinsCA	XP_016861127.1:n.2041-78_2041-77delinsCA
XM_017005639.1:c.2041-78_2041-77delinsCA	XP_016861128.1:n.2041-78_2041-77delinsCA
NM_001378259.1:c.3139-78_3139-77delinsCA	NP_001365188.1:n.3139-78_3139-77delinsCA
NM_183357.3:c.3064-78_3064-77delinsCA MANE Select	NP_899200.1:n.3064-78_3064-77delinsCA