Canonical Allele Identifier: CA418573168

Gene: NEXN

Linked Data

• dbSNP Id: rs1240780635
• gnomAD v2: 1-78407770-T-C
• gnomAD v4: 1-77942085-T-C
• MyVariant Identifiers: chr1:g.78407770T>C (hg19) ; chr1:g.77942085T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942085T>C , CM000663.2:g.77942085T>C	GRCh38
NC_000001.10:g.78407770T>C , CM000663.1:g.78407770T>C	GRCh37
NC_000001.9:g.78180358T>C	NCBI36
NG_016625.1:g.58571T>C , LRG_442:g.58571T>C
NG_033243.2:g.42009A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1536T>C MANE Select	ENSP00000333938.7:p.Asn512=
ENST00000330010.12:c.1344T>C	ENSP00000327363.8:p.Asn448=
ENST00000334785.11:c.1536T>C	ENSP00000333938.7:p.Asn512=
ENST00000342754.5:c.1235T>C
ENST00000470735.1:n.375T>C
ENST00000480732.2:n.1110T>C
NM_001172309.1:c.1344T>C	NP_001165780.1:p.Asn448=
NM_144573.3:c.1536T>C , LRG_442t1:c.1536T>C	NP_653174.3:p.Asn512=
XM_005271322.2:c.1536T>C	XP_005271379.1:p.Asn512=
XM_005271323.2:c.1494T>C	XP_005271380.1:p.Asn498=
XM_005271324.3:c.1344T>C	XP_005271381.1:p.Asn448=
XM_005271325.2:c.1314T>C	XP_005271382.1:p.Asn438=
XM_005271326.2:c.1302T>C	XP_005271383.1:p.Asn434=
XM_005271327.2:c.1119T>C	XP_005271384.1:p.Asn373=
XM_005271322.4:c.1536T>C	XP_005271379.1:p.Asn512=
XM_005271323.4:c.1494T>C	XP_005271380.1:p.Asn498=
XM_005271324.5:c.1344T>C	XP_005271381.1:p.Asn448=
XM_005271325.4:c.1314T>C	XP_005271382.1:p.Asn438=
XM_005271326.4:c.1302T>C	XP_005271383.1:p.Asn434=
XM_005271327.4:c.1119T>C	XP_005271384.1:p.Asn373=
NM_001172309.2:c.1344T>C	NP_001165780.1:p.Asn448=
NM_144573.4:c.1536T>C MANE Select	NP_653174.3:p.Asn512=