Canonical Allele Identifier: CA340878531

Gene: NEXN

Linked Data

• MyVariant Identifiers: chr1:g.78401566T>C (hg19) ; chr1:g.77935881T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77935881T>C , CM000663.2:g.77935881T>C	GRCh38
NC_000001.10:g.78401566T>C , CM000663.1:g.78401566T>C	GRCh37
NC_000001.9:g.78174154T>C	NCBI36
NG_016625.1:g.52367T>C , LRG_442:g.52367T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334785.12:c.1310T>C MANE Select	ENSP00000333938.7:p.Leu437Ser
ENST00000330010.12:c.1118T>C	ENSP00000327363.8:p.Leu373Ser
ENST00000334785.11:c.1310T>C	ENSP00000333938.7:p.Leu437Ser
ENST00000342754.5:c.1009T>C
ENST00000440324.5:c.1268T>C	ENSP00000411902.1:p.Leu423Ser
ENST00000464998.1:n.770T>C
ENST00000480732.2:n.884T>C
NM_001172309.1:c.1118T>C	NP_001165780.1:p.Leu373Ser
NM_144573.3:c.1310T>C , LRG_442t1:c.1310T>C	NP_653174.3:p.Leu437Ser
XM_005271322.2:c.1310T>C	XP_005271379.1:p.Leu437Ser
XM_005271323.2:c.1268T>C	XP_005271380.1:p.Leu423Ser
XM_005271324.3:c.1118T>C	XP_005271381.1:p.Leu373Ser
XM_005271325.2:c.1251+2402T>C	XP_005271382.1:n.1251+2402T>C
XM_005271326.2:c.1076T>C	XP_005271383.1:p.Leu359Ser
XM_005271327.2:c.893T>C	XP_005271384.1:p.Leu298Ser
XM_005271322.4:c.1310T>C	XP_005271379.1:p.Leu437Ser
XM_005271323.4:c.1268T>C	XP_005271380.1:p.Leu423Ser
XM_005271324.5:c.1118T>C	XP_005271381.1:p.Leu373Ser
XM_005271325.4:c.1251+2402T>C	XP_005271382.1:n.1251+2402T>C
XM_005271326.4:c.1076T>C	XP_005271383.1:p.Leu359Ser
XM_005271327.4:c.893T>C	XP_005271384.1:p.Leu298Ser
NM_001172309.2:c.1118T>C	NP_001165780.1:p.Leu373Ser
NM_144573.4:c.1310T>C MANE Select	NP_653174.3:p.Leu437Ser