Canonical Allele Identifier: CA739055435

Gene: NEXN

Linked Data

• dbSNP Id: rs1299274350
• gnomAD v3: 1-77936245-TTAAAACCTATAGTGAA-T
• gnomAD v4: 1-77936245-TTAAAACCTATAGTGAA-T
• MyVariant Identifiers: chr1:g.78401931_78401946del (hg19) ; chr1:g.77936246_77936261del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77936247_77936262del , CM000663.2:g.77936247_77936262del	GRCh38
NC_000001.10:g.78401932_78401947del , CM000663.1:g.78401932_78401947del	GRCh37
NC_000001.9:g.78174520_78174535del	NCBI36
NG_016625.1:g.52733_52748del , LRG_442:g.52733_52748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1473+203_1473+218del MANE Select	ENSP00000333938.7:n.1473+203_1473+218del
ENST00000330010.12:c.1281+203_1281+218del	ENSP00000327363.8:n.1281+203_1281+218del
ENST00000334785.11:c.1473+203_1473+218del	ENSP00000333938.7:n.1473+203_1473+218del
ENST00000342754.5:c.1172+203_1172+218del
ENST00000480732.2:n.1047+203_1047+218del
NM_001172309.1:c.1281+203_1281+218del	NP_001165780.1:n.1281+203_1281+218del
NM_144573.3:c.1473+203_1473+218del , LRG_442t1:c.1473+203_1473+218del	NP_653174.3:n.1473+203_1473+218del
XM_005271322.2:c.1473+203_1473+218del	XP_005271379.1:n.1473+203_1473+218del
XM_005271323.2:c.1431+203_1431+218del	XP_005271380.1:n.1431+203_1431+218del
XM_005271324.3:c.1281+203_1281+218del	XP_005271381.1:n.1281+203_1281+218del
XM_005271325.2:c.1251+2768_1251+2783del	XP_005271382.1:n.1251+2768_1251+2783del
XM_005271326.2:c.1239+203_1239+218del	XP_005271383.1:n.1239+203_1239+218del
XM_005271327.2:c.1056+203_1056+218del	XP_005271384.1:n.1056+203_1056+218del
XM_005271322.4:c.1473+203_1473+218del	XP_005271379.1:n.1473+203_1473+218del
XM_005271323.4:c.1431+203_1431+218del	XP_005271380.1:n.1431+203_1431+218del
XM_005271324.5:c.1281+203_1281+218del	XP_005271381.1:n.1281+203_1281+218del
XM_005271325.4:c.1251+2768_1251+2783del	XP_005271382.1:n.1251+2768_1251+2783del
XM_005271326.4:c.1239+203_1239+218del	XP_005271383.1:n.1239+203_1239+218del
XM_005271327.4:c.1056+203_1056+218del	XP_005271384.1:n.1056+203_1056+218del
NM_001172309.2:c.1281+203_1281+218del	NP_001165780.1:n.1281+203_1281+218del
NM_144573.4:c.1473+203_1473+218del MANE Select	NP_653174.3:n.1473+203_1473+218del