Canonical Allele Identifier: CA919030

Gene: NEXN

Linked Data

• dbSNP Id: rs754542219
• ExAC: 1:78408525 T / TAA
• gnomAD v2: 1-78408525-T-TAA
• MyVariant Identifiers: chr1:g.78408525_78408526insAA (hg19) ; chr1:g.77942840_77942841insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942841_77942842insAA , CM000663.2:g.77942841_77942842insAA	GRCh38
NC_000001.10:g.78408526_78408527insAA , CM000663.1:g.78408526_78408527insAA	GRCh37
NC_000001.9:g.78181114_78181115insAA	NCBI36
NG_016625.1:g.59327_59328insAA , LRG_442:g.59327_59328insAA
NG_033243.2:g.41253_41254insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*12_*13insAA MANE Select	ENSP00000333938.7:n.*12_*13insAA
ENST00000330010.12:c.*12_*13insAA	ENSP00000327363.8:n.*12_*13insAA
ENST00000334785.11:c.*12_*13insAA	ENSP00000333938.7:n.*12_*13insAA
ENST00000342754.5:c.1716+23_1716+24insAA
ENST00000480732.2:n.1614_1615insAA
NM_001172309.1:c.*12_*13insAA	NP_001165780.1:n.*12_*13insAA
NM_144573.3:c.*12_*13insAA , LRG_442t1:c.*12_*13insAA	NP_653174.3:n.*12_*13insAA
XM_005271322.2:c.2017+23_2017+24insAA	XP_005271379.1:n.2017+23_2017+24insAA
XM_005271323.2:c.1975+23_1975+24insAA	XP_005271380.1:n.1975+23_1975+24insAA
XM_005271324.3:c.1825+23_1825+24insAA	XP_005271381.1:n.1825+23_1825+24insAA
XM_005271325.2:c.1795+23_1795+24insAA	XP_005271382.1:n.1795+23_1795+24insAA
XM_005271326.2:c.1783+23_1783+24insAA	XP_005271383.1:n.1783+23_1783+24insAA
XM_005271327.2:c.1600+23_1600+24insAA	XP_005271384.1:n.1600+23_1600+24insAA
XM_005271322.4:c.2017+23_2017+24insAA	XP_005271379.1:n.2017+23_2017+24insAA
XM_005271323.4:c.1975+23_1975+24insAA	XP_005271380.1:n.1975+23_1975+24insAA
XM_005271324.5:c.1825+23_1825+24insAA	XP_005271381.1:n.1825+23_1825+24insAA
XM_005271325.4:c.1795+23_1795+24insAA	XP_005271382.1:n.1795+23_1795+24insAA
XM_005271326.4:c.1783+23_1783+24insAA	XP_005271383.1:n.1783+23_1783+24insAA
XM_005271327.4:c.1600+23_1600+24insAA	XP_005271384.1:n.1600+23_1600+24insAA
NM_001172309.2:c.*12_*13insAA	NP_001165780.1:n.*12_*13insAA
NM_144573.4:c.*12_*13insAA MANE Select	NP_653174.3:n.*12_*13insAA