Canonical Allele Identifier: CA340883779

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78408509A>C (hg19) ; chr1:g.77942824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942824A>C , CM000663.2:g.77942824A>C	GRCh38
NC_000001.10:g.78408509A>C , CM000663.1:g.78408509A>C	GRCh37
NC_000001.9:g.78181097A>C	NCBI36
NG_016625.1:g.59310A>C , LRG_442:g.59310A>C
NG_033243.2:g.41270T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.2023A>C MANE Select	ENSP00000333938.7:p.Asn675His
ENST00000330010.12:c.1831A>C	ENSP00000327363.8:p.Asn611His
ENST00000334785.11:c.2023A>C	ENSP00000333938.7:p.Asn675His
ENST00000342754.5:c.1716+6A>C
ENST00000480732.2:n.1597A>C
NM_001172309.1:c.1831A>C	NP_001165780.1:p.Asn611His
NM_144573.3:c.2023A>C , LRG_442t1:c.2023A>C	NP_653174.3:p.Asn675His
XM_005271322.2:c.2017+6A>C	XP_005271379.1:n.2017+6A>C
XM_005271323.2:c.1975+6A>C	XP_005271380.1:n.1975+6A>C
XM_005271324.3:c.1825+6A>C	XP_005271381.1:n.1825+6A>C
XM_005271325.2:c.1795+6A>C	XP_005271382.1:n.1795+6A>C
XM_005271326.2:c.1783+6A>C	XP_005271383.1:n.1783+6A>C
XM_005271327.2:c.1600+6A>C	XP_005271384.1:n.1600+6A>C
XM_005271322.4:c.2017+6A>C	XP_005271379.1:n.2017+6A>C
XM_005271323.4:c.1975+6A>C	XP_005271380.1:n.1975+6A>C
XM_005271324.5:c.1825+6A>C	XP_005271381.1:n.1825+6A>C
XM_005271325.4:c.1795+6A>C	XP_005271382.1:n.1795+6A>C
XM_005271326.4:c.1783+6A>C	XP_005271383.1:n.1783+6A>C
XM_005271327.4:c.1600+6A>C	XP_005271384.1:n.1600+6A>C
NM_001172309.2:c.1831A>C	NP_001165780.1:p.Asn611His
NM_144573.4:c.2023A>C MANE Select	NP_653174.3:p.Asn675His