Canonical Allele Identifier: CA418709840

Gene: NEXN

Linked Data

• gnomAD v4: 1-77942772-C-A
• MyVariant Identifiers: chr1:g.78408457C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77942772C>A , CM000663.2:g.77942772C>A	GRCh38
NC_000001.10:g.78408457C>A , CM000663.1:g.78408457C>A	GRCh37
NC_000001.9:g.78181045C>A	NCBI36
NG_016625.1:g.59258C>A , LRG_442:g.59258C>A
NG_033243.2:g.41322G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.1971C>A MANE Select	ENSP00000333938.7:p.Val657=
ENST00000330010.12:c.1779C>A	ENSP00000327363.8:p.Val593=
ENST00000334785.11:c.1971C>A	ENSP00000333938.7:p.Val657=
ENST00000342754.5:c.1670C>A
ENST00000480732.2:n.1545C>A
NM_001172309.1:c.1779C>A	NP_001165780.1:p.Val593=
NM_144573.3:c.1971C>A , LRG_442t1:c.1971C>A	NP_653174.3:p.Val657=
XM_005271322.2:c.1971C>A	XP_005271379.1:p.Val657=
XM_005271323.2:c.1929C>A	XP_005271380.1:p.Val643=
XM_005271324.3:c.1779C>A	XP_005271381.1:p.Val593=
XM_005271325.2:c.1749C>A	XP_005271382.1:p.Val583=
XM_005271326.2:c.1737C>A	XP_005271383.1:p.Val579=
XM_005271327.2:c.1554C>A	XP_005271384.1:p.Val518=
XM_005271322.4:c.1971C>A	XP_005271379.1:p.Val657=
XM_005271323.4:c.1929C>A	XP_005271380.1:p.Val643=
XM_005271324.5:c.1779C>A	XP_005271381.1:p.Val593=
XM_005271325.4:c.1749C>A	XP_005271382.1:p.Val583=
XM_005271326.4:c.1737C>A	XP_005271383.1:p.Val579=
XM_005271327.4:c.1554C>A	XP_005271384.1:p.Val518=
NM_001172309.2:c.1779C>A	NP_001165780.1:p.Val593=
NM_144573.4:c.1971C>A MANE Select	NP_653174.3:p.Val657=