Canonical Allele Identifier: CA898159439

Gene: ADCY5

Linked Data

• dbSNP Id: rs1291667760
• gnomAD v3: 3-123291438-ACCTCCT-A
• gnomAD v4: 3-123291438-ACCTCCT-A
• MyVariant Identifiers: chr3:g.123010286_123010291del (hg19) ; chr3:g.123291439_123291444del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291443_123291448del , CM000665.2:g.123291443_123291448del	GRCh38
NC_000003.11:g.123010290_123010295del , CM000665.1:g.123010290_123010295del	GRCh37
NC_000003.10:g.124492980_124492985del	NCBI36
NG_033882.1:g.162102_162107del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1741-68_1741-63del	ENSP00000420082.2:n.1741-68_1741-63del
ENST00000470367.2:c.2029-68_2029-63del	ENSP00000514541.1:n.2029-68_2029-63del
ENST00000483566.2:c.1741-68_1741-63del	ENSP00000420252.2:n.1741-68_1741-63del
ENST00000699714.1:c.1741-68_1741-63del	ENSP00000514539.1:n.1741-68_1741-63del
ENST00000699715.1:c.1741-68_1741-63del	ENSP00000514540.1:n.1741-68_1741-63del
ENST00000699716.1:c.1741-68_1741-63del	ENSP00000514542.1:n.1741-68_1741-63del
ENST00000699717.1:n.1467-68_1467-63del
ENST00000699718.1:c.3139-68_3139-63del	ENSP00000514543.1:n.3139-68_3139-63del
ENST00000462833.6:c.3064-68_3064-63del MANE Select	ENSP00000419361.1:n.3064-68_3064-63del
ENST00000309879.9:c.2014-68_2014-63del	ENSP00000308685.5:n.2014-68_2014-63del
ENST00000462833.5:c.3064-68_3064-63del	ENSP00000419361.1:n.3064-68_3064-63del
ENST00000491190.5:c.2038-68_2038-63del	ENSP00000418537.1:n.2038-68_2038-63del
NM_001199642.1:c.2014-68_2014-63del	NP_001186571.1:n.2014-68_2014-63del
NM_183357.2:c.3064-68_3064-63del	NP_899200.1:n.3064-68_3064-63del
XM_005247077.2:c.3139-68_3139-63del	XP_005247134.1:n.3139-68_3139-63del
XM_005247078.1:c.2089-68_2089-63del	XP_005247135.1:n.2089-68_2089-63del
XM_006713483.1:c.2038-68_2038-63del	XP_006713546.1:n.2038-68_2038-63del
XM_006713484.1:c.1816-68_1816-63del	XP_006713547.1:n.1816-68_1816-63del
XM_011512359.1:c.2140-68_2140-63del	XP_011510661.1:n.2140-68_2140-63del
XM_011512360.1:c.2050-68_2050-63del	XP_011510662.1:n.2050-68_2050-63del
XM_011512361.1:c.1816-68_1816-63del	XP_011510663.1:n.1816-68_1816-63del
XM_005247077.4:c.3139-68_3139-63del	XP_005247134.1:n.3139-68_3139-63del
XM_011512359.2:c.2140-68_2140-63del	XP_011510661.1:n.2140-68_2140-63del
XM_011512360.3:c.2050-68_2050-63del	XP_011510662.1:n.2050-68_2050-63del
XM_017005638.1:c.2041-68_2041-63del	XP_016861127.1:n.2041-68_2041-63del
XM_017005639.1:c.2041-68_2041-63del	XP_016861128.1:n.2041-68_2041-63del
NM_001378259.1:c.3139-68_3139-63del	NP_001365188.1:n.3139-68_3139-63del
NM_183357.3:c.3064-68_3064-63del MANE Select	NP_899200.1:n.3064-68_3064-63del