Canonical Allele Identifier: CA739053012

Gene: NEXN

Linked Data

• dbSNP Id: rs1266694169
• MyVariant Identifiers: chr1:g.78398922T>C (hg19) ; chr1:g.77933237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933237T>C , CM000663.2:g.77933237T>C	GRCh38
NC_000001.10:g.78398922T>C , CM000663.1:g.78398922T>C	GRCh37
NC_000001.9:g.78171510T>C	NCBI36
NG_016625.1:g.49723T>C , LRG_442:g.49723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1054-45T>C MANE Select	ENSP00000333938.7:n.1054-45T>C
ENST00000330010.12:c.862-45T>C	ENSP00000327363.8:n.862-45T>C
ENST00000334785.11:c.1054-45T>C	ENSP00000333938.7:n.1054-45T>C
ENST00000342754.5:c.753-45T>C
ENST00000401035.7:c.862-45T>C	ENSP00000383814.3:n.862-45T>C
ENST00000440324.5:c.1012-45T>C	ENSP00000411902.1:n.1012-45T>C
ENST00000464998.1:n.514-45T>C
ENST00000480732.2:n.583T>C
NM_001172309.1:c.862-45T>C	NP_001165780.1:n.862-45T>C
NM_144573.3:c.1054-45T>C , LRG_442t1:c.1054-45T>C	NP_653174.3:n.1054-45T>C
XM_005271322.2:c.1054-45T>C	XP_005271379.1:n.1054-45T>C
XM_005271323.2:c.1012-45T>C	XP_005271380.1:n.1012-45T>C
XM_005271324.3:c.862-45T>C	XP_005271381.1:n.862-45T>C
XM_005271325.2:c.1054-45T>C	XP_005271382.1:n.1054-45T>C
XM_005271326.2:c.820-45T>C	XP_005271383.1:n.820-45T>C
XM_005271327.2:c.637-45T>C	XP_005271384.1:n.637-45T>C
XM_005271322.4:c.1054-45T>C	XP_005271379.1:n.1054-45T>C
XM_005271323.4:c.1012-45T>C	XP_005271380.1:n.1012-45T>C
XM_005271324.5:c.862-45T>C	XP_005271381.1:n.862-45T>C
XM_005271325.4:c.1054-45T>C	XP_005271382.1:n.1054-45T>C
XM_005271326.4:c.820-45T>C	XP_005271383.1:n.820-45T>C
XM_005271327.4:c.637-45T>C	XP_005271384.1:n.637-45T>C
NM_001172309.2:c.862-45T>C	NP_001165780.1:n.862-45T>C
NM_144573.4:c.1054-45T>C MANE Select	NP_653174.3:n.1054-45T>C