Canonical Allele Identifier: CA24683998

Gene: NEXN

Linked Data

• dbSNP Id: rs917490518
• gnomAD v2: 1-78398876-C-CA
• gnomAD v3: 1-77933191-C-CA
• gnomAD v4: 1-77933191-C-CA
• MyVariant Identifiers: chr1:g.78398876_78398877insA (hg19) ; chr1:g.77933191_77933192insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77933199dup , CM000663.2:g.77933199dup	GRCh38
NC_000001.10:g.78398884dup , CM000663.1:g.78398884dup	GRCh37
NC_000001.9:g.78171472dup	NCBI36
NG_016625.1:g.49685dup , LRG_442:g.49685dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1054-83dup MANE Select	ENSP00000333938.7:n.1054-83dup
ENST00000330010.12:c.862-83dup	ENSP00000327363.8:n.862-83dup
ENST00000334785.11:c.1054-83dup	ENSP00000333938.7:n.1054-83dup
ENST00000342754.5:c.753-83dup
ENST00000401035.7:c.862-83dup	ENSP00000383814.3:n.862-83dup
ENST00000440324.5:c.1012-83dup	ENSP00000411902.1:n.1012-83dup
ENST00000464998.1:n.514-83dup
ENST00000480732.2:n.545dup
NM_001172309.1:c.862-83dup	NP_001165780.1:n.862-83dup
NM_144573.3:c.1054-83dup , LRG_442t1:c.1054-83dup	NP_653174.3:n.1054-83dup
XM_005271322.2:c.1054-83dup	XP_005271379.1:n.1054-83dup
XM_005271323.2:c.1012-83dup	XP_005271380.1:n.1012-83dup
XM_005271324.3:c.862-83dup	XP_005271381.1:n.862-83dup
XM_005271325.2:c.1054-83dup	XP_005271382.1:n.1054-83dup
XM_005271326.2:c.820-83dup	XP_005271383.1:n.820-83dup
XM_005271327.2:c.637-83dup	XP_005271384.1:n.637-83dup
XM_005271322.4:c.1054-83dup	XP_005271379.1:n.1054-83dup
XM_005271323.4:c.1012-83dup	XP_005271380.1:n.1012-83dup
XM_005271324.5:c.862-83dup	XP_005271381.1:n.862-83dup
XM_005271325.4:c.1054-83dup	XP_005271382.1:n.1054-83dup
XM_005271326.4:c.820-83dup	XP_005271383.1:n.820-83dup
XM_005271327.4:c.637-83dup	XP_005271384.1:n.637-83dup
NM_001172309.2:c.862-83dup	NP_001165780.1:n.862-83dup
NM_144573.4:c.1054-83dup MANE Select	NP_653174.3:n.1054-83dup