Canonical Allele Identifier: CA2576692124

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823141-CTATTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823142_24823147del , CM000664.2:g.24823142_24823147del	GRCh38
NC_000002.11:g.25046011_25046016del , CM000664.1:g.25046011_25046016del	GRCh37
NC_000002.10:g.24899515_24899520del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2886+62_2886+67del	ENSP00000384484.2:n.2886+62_2886+67del
ENST00000679454.1:c.2883+62_2883+67del MANE Select	ENSP00000505261.1:n.2883+62_2883+67del
ENST00000260600.9:c.2883+62_2883+67del	ENSP00000260600.5:n.2883+62_2883+67del
ENST00000405392.5:c.2886+62_2886+67del	ENSP00000384484.2:n.2886+62_2886+67del
ENST00000485887.1:n.155+62_155+67del
ENST00000606682.5:c.1824+62_1824+67del	ENSP00000475652.1:n.1824+62_1824+67del
NM_004036.3:c.2883+62_2883+67del	NP_004027.2:n.2883+62_2883+67del
XM_005264104.1:c.2886+62_2886+67del	XP_005264161.1:n.2886+62_2886+67del
XM_005264105.1:c.2883+62_2883+67del	XP_005264162.1:n.2883+62_2883+67del
XM_006711925.1:c.2952+62_2952+67del	XP_006711988.1:n.2952+62_2952+67del
XM_011532489.1:c.3009+62_3009+67del	XP_011530791.1:n.3009+62_3009+67del
XM_011532490.1:c.3006+62_3006+67del	XP_011530792.1:n.3006+62_3006+67del
XM_011532491.1:c.2943+62_2943+67del	XP_011530793.1:n.2943+62_2943+67del
XM_011532492.1:c.3009+62_3009+67del	XP_011530794.1:n.3009+62_3009+67del
XM_011532493.1:c.2871+62_2871+67del	XP_011530795.1:n.2871+62_2871+67del
XM_011532494.1:c.2811+62_2811+67del	XP_011530796.1:n.2811+62_2811+67del
XM_011532495.1:c.2343+62_2343+67del	XP_011530797.1:n.2343+62_2343+67del
XM_011532496.1:c.2286+62_2286+67del	XP_011530798.1:n.2286+62_2286+67del
NM_001320613.1:c.2886+62_2886+67del	NP_001307542.1:n.2886+62_2886+67del
NM_004036.4:c.2883+62_2883+67del	NP_004027.2:n.2883+62_2883+67del
XM_011532492.2:c.3009+62_3009+67del	XP_011530794.1:n.3009+62_3009+67del
XM_017003186.1:c.2949+62_2949+67del	XP_016858675.1:n.2949+62_2949+67del
XM_017003187.1:c.2940+62_2940+67del	XP_016858676.1:n.2940+62_2940+67del
XM_017003188.1:c.3006+62_3006+67del	XP_016858677.1:n.3006+62_3006+67del
XM_017003189.1:c.2868+62_2868+67del	XP_016858678.1:n.2868+62_2868+67del
XM_017003190.1:c.2745+62_2745+67del	XP_016858679.1:n.2745+62_2745+67del
XM_017003191.1:c.2373+62_2373+67del	XP_016858680.1:n.2373+62_2373+67del
XM_017003192.1:c.2163+62_2163+67del	XP_016858681.1:n.2163+62_2163+67del
XM_017003193.1:c.2160+62_2160+67del	XP_016858682.1:n.2160+62_2160+67del
NM_001320613.2:c.2886+62_2886+67del	NP_001307542.1:n.2886+62_2886+67del
NM_001377128.1:c.2949+62_2949+67del	NP_001364057.1:n.2949+62_2949+67del
NM_001377129.1:c.2745+62_2745+67del	NP_001364058.1:n.2745+62_2745+67del
NM_001377130.1:c.2332-517_2332-512del	NP_001364059.1:n.2332-517_2332-512del
NM_001377131.1:c.2160+62_2160+67del	NP_001364060.1:n.2160+62_2160+67del
NM_001377132.1:c.2883+62_2883+67del	NP_001364061.1:n.2883+62_2883+67del
NM_004036.5:c.2883+62_2883+67del MANE Select	NP_004027.2:n.2883+62_2883+67del