Canonical Allele Identifier: CA918547

Gene: NEXN

Linked Data

• dbSNP Id: rs753831137
• ExAC: 1:78383204 CCTAT / C
• gnomAD v2: 1-78383204-CCTAT-C
• gnomAD v3: 1-77917519-CCTAT-C
• gnomAD v4: 1-77917519-CCTAT-C
• MyVariant Identifiers: chr1:g.78383205_78383208del (hg19) ; chr1:g.77917520_77917523del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77917522_77917525del , CM000663.2:g.77917522_77917525del	GRCh38
NC_000001.10:g.78383207_78383210del , CM000663.1:g.78383207_78383210del	GRCh37
NC_000001.9:g.78155795_78155798del	NCBI36
NG_016625.1:g.34008_34011del , LRG_442:g.34008_34011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.28-44_28-41del MANE Select	ENSP00000333938.7:n.28-44_28-41del
ENST00000330010.12:c.28-438_28-435del	ENSP00000327363.8:n.28-438_28-435del
ENST00000334785.11:c.28-44_28-41del	ENSP00000333938.7:n.28-44_28-41del
ENST00000401035.7:c.28-438_28-435del	ENSP00000383814.3:n.28-438_28-435del
ENST00000440324.5:c.28-44_28-41del	ENSP00000411902.1:n.28-44_28-41del
NM_001172309.1:c.28-438_28-435del	NP_001165780.1:n.28-438_28-435del
NM_144573.3:c.28-44_28-41del , LRG_442t1:c.28-44_28-41del	NP_653174.3:n.28-44_28-41del
XM_005271322.2:c.28-44_28-41del	XP_005271379.1:n.28-44_28-41del
XM_005271323.2:c.28-44_28-41del	XP_005271380.1:n.28-44_28-41del
XM_005271324.3:c.28-438_28-435del	XP_005271381.1:n.28-438_28-435del
XM_005271325.2:c.28-44_28-41del	XP_005271382.1:n.28-44_28-41del
XM_005271326.2:c.28-438_28-435del	XP_005271383.1:n.28-438_28-435del
XM_005271327.2:c.28-44_28-41del	XP_005271384.1:n.28-44_28-41del
XM_005271322.4:c.28-44_28-41del	XP_005271379.1:n.28-44_28-41del
XM_005271323.4:c.28-44_28-41del	XP_005271380.1:n.28-44_28-41del
XM_005271324.5:c.28-438_28-435del	XP_005271381.1:n.28-438_28-435del
XM_005271325.4:c.28-44_28-41del	XP_005271382.1:n.28-44_28-41del
XM_005271326.4:c.28-438_28-435del	XP_005271383.1:n.28-438_28-435del
XM_005271327.4:c.28-44_28-41del	XP_005271384.1:n.28-44_28-41del
NM_001172309.2:c.28-438_28-435del	NP_001165780.1:n.28-438_28-435del
NM_144573.4:c.28-44_28-41del MANE Select	NP_653174.3:n.28-44_28-41del