Canonical Allele Identifier: CA340883672

Gene: NEXN

Linked Data

• COSMIC: COSM3741383 ; COSM3741384
• MyVariant Identifiers: chr1:g.78408473G>C (hg19) ; chr1:g.77942788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942788G>C , CM000663.2:g.77942788G>C	GRCh38
NC_000001.10:g.78408473G>C , CM000663.1:g.78408473G>C	GRCh37
NC_000001.9:g.78181061G>C	NCBI36
NG_016625.1:g.59274G>C , LRG_442:g.59274G>C
NG_033243.2:g.41306C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1987G>C MANE Select	ENSP00000333938.7:p.Ala663Pro
ENST00000330010.12:c.1795G>C	ENSP00000327363.8:p.Ala599Pro
ENST00000334785.11:c.1987G>C	ENSP00000333938.7:p.Ala663Pro
ENST00000342754.5:c.1686G>C
ENST00000480732.2:n.1561G>C
NM_001172309.1:c.1795G>C	NP_001165780.1:p.Ala599Pro
NM_144573.3:c.1987G>C , LRG_442t1:c.1987G>C	NP_653174.3:p.Ala663Pro
XM_005271322.2:c.1987G>C	XP_005271379.1:p.Ala663Pro
XM_005271323.2:c.1945G>C	XP_005271380.1:p.Ala649Pro
XM_005271324.3:c.1795G>C	XP_005271381.1:p.Ala599Pro
XM_005271325.2:c.1765G>C	XP_005271382.1:p.Ala589Pro
XM_005271326.2:c.1753G>C	XP_005271383.1:p.Ala585Pro
XM_005271327.2:c.1570G>C	XP_005271384.1:p.Ala524Pro
XM_005271322.4:c.1987G>C	XP_005271379.1:p.Ala663Pro
XM_005271323.4:c.1945G>C	XP_005271380.1:p.Ala649Pro
XM_005271324.5:c.1795G>C	XP_005271381.1:p.Ala599Pro
XM_005271325.4:c.1765G>C	XP_005271382.1:p.Ala589Pro
XM_005271326.4:c.1753G>C	XP_005271383.1:p.Ala585Pro
XM_005271327.4:c.1570G>C	XP_005271384.1:p.Ala524Pro
NM_001172309.2:c.1795G>C	NP_001165780.1:p.Ala599Pro
NM_144573.4:c.1987G>C MANE Select	NP_653174.3:p.Ala663Pro