Canonical Allele Identifier: CA1177626539

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943040_77943042delinsAAC , CM000663.2:g.77943040_77943042delinsAAC	GRCh38
NC_000001.10:g.78408725_78408727delinsAAC , CM000663.1:g.78408725_78408727delinsAAC	GRCh37
NC_000001.9:g.78181313_78181315delinsAAC	NCBI36
NG_016625.1:g.59526_59528delinsAAC , LRG_442:g.59526_59528delinsAAC
NG_033243.2:g.41052_41054delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*211_*213delinsAAC MANE Select	ENSP00000333938.7:n.*211_*213delinsAAC
ENST00000330010.12:c.*211_*213delinsAAC	ENSP00000327363.8:n.*211_*213delinsAAC
ENST00000334785.11:c.*211_*213delinsAAC	ENSP00000333938.7:n.*211_*213delinsAAC
ENST00000342754.5:c.1857_1859delinsAAC
ENST00000480732.2:n.1813_1815delinsAAC
NM_001172309.1:c.*211_*213delinsAAC	NP_001165780.1:n.*211_*213delinsAAC
NM_144573.3:c.*211_*213delinsAAC , LRG_442t1:c.*211_*213delinsAAC	NP_653174.3:n.*211_*213delinsAAC
XM_005271322.2:c.*127_*129delinsAAC	XP_005271379.1:n.*127_*129delinsAAC
XM_005271323.2:c.*127_*129delinsAAC	XP_005271380.1:n.*127_*129delinsAAC
XM_005271324.3:c.*127_*129delinsAAC	XP_005271381.1:n.*127_*129delinsAAC
XM_005271325.2:c.*127_*129delinsAAC	XP_005271382.1:n.*127_*129delinsAAC
XM_005271326.2:c.*127_*129delinsAAC	XP_005271383.1:n.*127_*129delinsAAC
XM_005271327.2:c.*127_*129delinsAAC	XP_005271384.1:n.*127_*129delinsAAC
XM_005271322.4:c.*127_*129delinsAAC	XP_005271379.1:n.*127_*129delinsAAC
XM_005271323.4:c.*127_*129delinsAAC	XP_005271380.1:n.*127_*129delinsAAC
XM_005271324.5:c.*127_*129delinsAAC	XP_005271381.1:n.*127_*129delinsAAC
XM_005271325.4:c.*127_*129delinsAAC	XP_005271382.1:n.*127_*129delinsAAC
XM_005271326.4:c.*127_*129delinsAAC	XP_005271383.1:n.*127_*129delinsAAC
XM_005271327.4:c.*127_*129delinsAAC	XP_005271384.1:n.*127_*129delinsAAC
NM_001172309.2:c.*211_*213delinsAAC	NP_001165780.1:n.*211_*213delinsAAC
NM_144573.4:c.*211_*213delinsAAC MANE Select	NP_653174.3:n.*211_*213delinsAAC