Canonical Allele Identifier: CA340874994

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78395011A>C (hg19) ; chr1:g.77929326A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77929326A>C , CM000663.2:g.77929326A>C	GRCh38
NC_000001.10:g.78395011A>C , CM000663.1:g.78395011A>C	GRCh37
NC_000001.9:g.78167599A>C	NCBI36
NG_016625.1:g.45812A>C , LRG_442:g.45812A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.875A>C MANE Select	ENSP00000333938.7:p.Asp292Ala
ENST00000330010.12:c.683A>C	ENSP00000327363.8:p.Asp228Ala
ENST00000334785.11:c.875A>C	ENSP00000333938.7:p.Asp292Ala
ENST00000342754.5:c.574A>C
ENST00000401035.7:c.683A>C	ENSP00000383814.3:p.Asp228Ala
ENST00000440324.5:c.833A>C	ENSP00000411902.1:p.Asp278Ala
ENST00000464998.1:n.335A>C
NM_001172309.1:c.683A>C	NP_001165780.1:p.Asp228Ala
NM_144573.3:c.875A>C , LRG_442t1:c.875A>C	NP_653174.3:p.Asp292Ala
XM_005271322.2:c.875A>C	XP_005271379.1:p.Asp292Ala
XM_005271323.2:c.833A>C	XP_005271380.1:p.Asp278Ala
XM_005271324.3:c.683A>C	XP_005271381.1:p.Asp228Ala
XM_005271325.2:c.875A>C	XP_005271382.1:p.Asp292Ala
XM_005271326.2:c.641A>C	XP_005271383.1:p.Asp214Ala
XM_005271327.2:c.458A>C	XP_005271384.1:p.Asp153Ala
XM_005271322.4:c.875A>C	XP_005271379.1:p.Asp292Ala
XM_005271323.4:c.833A>C	XP_005271380.1:p.Asp278Ala
XM_005271324.5:c.683A>C	XP_005271381.1:p.Asp228Ala
XM_005271325.4:c.875A>C	XP_005271382.1:p.Asp292Ala
XM_005271326.4:c.641A>C	XP_005271383.1:p.Asp214Ala
XM_005271327.4:c.458A>C	XP_005271384.1:p.Asp153Ala
NM_001172309.2:c.683A>C	NP_001165780.1:p.Asp228Ala
NM_144573.4:c.875A>C MANE Select	NP_653174.3:p.Asp292Ala