Canonical Allele Identifier: CA2581634210

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943108G>C , CM000663.2:g.77943108G>C	GRCh38
NC_000001.10:g.78408793G>C , CM000663.1:g.78408793G>C	GRCh37
NC_000001.9:g.78181381G>C	NCBI36
NG_016625.1:g.59594G>C , LRG_442:g.59594G>C
NG_033243.2:g.40986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*279G>C MANE Select	ENSP00000333938.7:n.*279G>C
ENST00000330010.12:c.*279G>C	ENSP00000327363.8:n.*279G>C
ENST00000334785.11:c.*279G>C	ENSP00000333938.7:n.*279G>C
ENST00000342754.5:c.1925G>C
ENST00000480732.2:n.1881G>C
NM_001172309.1:c.*279G>C	NP_001165780.1:n.*279G>C
NM_144573.3:c.*279G>C , LRG_442t1:c.*279G>C	NP_653174.3:n.*279G>C
XM_005271322.2:c.*195G>C	XP_005271379.1:n.*195G>C
XM_005271323.2:c.*195G>C	XP_005271380.1:n.*195G>C
XM_005271324.3:c.*195G>C	XP_005271381.1:n.*195G>C
XM_005271325.2:c.*195G>C	XP_005271382.1:n.*195G>C
XM_005271326.2:c.*195G>C	XP_005271383.1:n.*195G>C
XM_005271327.2:c.*195G>C	XP_005271384.1:n.*195G>C
XM_005271322.4:c.*195G>C	XP_005271379.1:n.*195G>C
XM_005271323.4:c.*195G>C	XP_005271380.1:n.*195G>C
XM_005271324.5:c.*195G>C	XP_005271381.1:n.*195G>C
XM_005271325.4:c.*195G>C	XP_005271382.1:n.*195G>C
XM_005271326.4:c.*195G>C	XP_005271383.1:n.*195G>C
XM_005271327.4:c.*195G>C	XP_005271384.1:n.*195G>C
NM_001172309.2:c.*279G>C	NP_001165780.1:n.*279G>C
NM_144573.4:c.*279G>C MANE Select	NP_653174.3:n.*279G>C