Canonical Allele Identifier: CA2646303553

Gene: NEXN

Linked Data

• gnomAD v4: 1-77918105-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77918105T>C , CM000663.2:g.77918105T>C	GRCh38
NC_000001.10:g.78383790T>C , CM000663.1:g.78383790T>C	GRCh37
NC_000001.9:g.78156378T>C	NCBI36
NG_016625.1:g.34591T>C , LRG_442:g.34591T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.299-20T>C MANE Select	ENSP00000333938.7:n.299-20T>C
ENST00000330010.12:c.107-20T>C	ENSP00000327363.8:n.107-20T>C
ENST00000334785.11:c.299-20T>C	ENSP00000333938.7:n.299-20T>C
ENST00000401035.7:c.107-20T>C	ENSP00000383814.3:n.107-20T>C
ENST00000440324.5:c.299-20T>C	ENSP00000411902.1:n.299-20T>C
NM_001172309.1:c.107-20T>C	NP_001165780.1:n.107-20T>C
NM_144573.3:c.299-20T>C , LRG_442t1:c.299-20T>C	NP_653174.3:n.299-20T>C
XM_005271322.2:c.299-20T>C	XP_005271379.1:n.299-20T>C
XM_005271323.2:c.299-20T>C	XP_005271380.1:n.299-20T>C
XM_005271324.3:c.107-20T>C	XP_005271381.1:n.107-20T>C
XM_005271325.2:c.299-20T>C	XP_005271382.1:n.299-20T>C
XM_005271326.2:c.107-20T>C	XP_005271383.1:n.107-20T>C
XM_005271327.2:c.299-20T>C	XP_005271384.1:n.299-20T>C
XM_005271322.4:c.299-20T>C	XP_005271379.1:n.299-20T>C
XM_005271323.4:c.299-20T>C	XP_005271380.1:n.299-20T>C
XM_005271324.5:c.107-20T>C	XP_005271381.1:n.107-20T>C
XM_005271325.4:c.299-20T>C	XP_005271382.1:n.299-20T>C
XM_005271326.4:c.107-20T>C	XP_005271383.1:n.107-20T>C
XM_005271327.4:c.299-20T>C	XP_005271384.1:n.299-20T>C
NM_001172309.2:c.107-20T>C	NP_001165780.1:n.107-20T>C
NM_144573.4:c.299-20T>C MANE Select	NP_653174.3:n.299-20T>C