Canonical Allele Identifier: CA1003481508

Gene: NEXN

Linked Data

• gnomAD v3: 1-77933522-C-CTATATTCCCCATATTTATTAAGG
• gnomAD v4: 1-77933522-C-CTATATTCCCCATATTTATTAAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933524_77933525insTATTCCCCATATTTATTAAGGTA , CM000663.2:g.77933524_77933525insTATTCCCCATATTTATTAAGGTA	GRCh38
NC_000001.10:g.78399209_78399210insTATTCCCCATATTTATTAAGGTA , CM000663.1:g.78399209_78399210insTATTCCCCATATTTATTAAGGTA	GRCh37
NC_000001.9:g.78171797_78171798insTATTCCCCATATTTATTAAGGTA	NCBI36
NG_016625.1:g.50010_50011insTATTCCCCATATTTATTAAGGTA , LRG_442:g.50010_50011insTATTCCCCATATTTATTAAGGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA MANE Select	ENSP00000333938.7:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA...
ENST00000330010.12:c.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA	ENSP00000327363.8:n.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA...
ENST00000334785.11:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA	ENSP00000333938.7:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA...
ENST00000342754.5:c.950+45_950+46insTATTCCCCATATTTATTAAGGTA
ENST00000440324.5:c.1209+45_1209+46insTATTCCCCATATTTATTAAGGTA	ENSP00000411902.1:n.1209+45_1209+46insTATTCCCCATATTTATTAAGGTA...
ENST00000464998.1:n.711+45_711+46insTATTCCCCATATTTATTAAGGTA
ENST00000480732.2:n.825+45_825+46insTATTCCCCATATTTATTAAGGTA
NM_001172309.1:c.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA	NP_001165780.1:n.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA
NM_144573.3:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA , LRG_442t1:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA	NP_653174.3:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA
XM_005271322.2:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA	XP_005271379.1:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA
XM_005271323.2:c.1209+45_1209+46insTATTCCCCATATTTATTAAGGTA	XP_005271380.1:n.1209+45_1209+46insTATTCCCCATATTTATTAAGGTA
XM_005271324.3:c.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA	XP_005271381.1:n.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA
XM_005271325.2:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA	XP_005271382.1:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA
XM_005271326.2:c.1017+45_1017+46insTATTCCCCATATTTATTAAGGTA	XP_005271383.1:n.1017+45_1017+46insTATTCCCCATATTTATTAAGGTA
XM_005271327.2:c.834+45_834+46insTATTCCCCATATTTATTAAGGTA	XP_005271384.1:n.834+45_834+46insTATTCCCCATATTTATTAAGGTA
XM_005271322.4:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA	XP_005271379.1:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA
XM_005271323.4:c.1209+45_1209+46insTATTCCCCATATTTATTAAGGTA	XP_005271380.1:n.1209+45_1209+46insTATTCCCCATATTTATTAAGGTA
XM_005271324.5:c.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA	XP_005271381.1:n.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA
XM_005271325.4:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA	XP_005271382.1:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA
XM_005271326.4:c.1017+45_1017+46insTATTCCCCATATTTATTAAGGTA	XP_005271383.1:n.1017+45_1017+46insTATTCCCCATATTTATTAAGGTA
XM_005271327.4:c.834+45_834+46insTATTCCCCATATTTATTAAGGTA	XP_005271384.1:n.834+45_834+46insTATTCCCCATATTTATTAAGGTA
NM_001172309.2:c.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA	NP_001165780.1:n.1059+45_1059+46insTATTCCCCATATTTATTAAGGTA
NM_144573.4:c.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA MANE Select	NP_653174.3:n.1251+45_1251+46insTATTCCCCATATTTATTAAGGTA