Canonical Allele Identifier: CA2242560857

Gene: NXN

Linked Data

• dbSNP Id: rs12603526

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.897353T>G , CM000679.2:g.897353T>G	GRCh38
NC_000017.10:g.800593T>G , CM000679.1:g.800593T>G	GRCh37
NC_000017.9:g.747343T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336868.8:c.361-71275A>C MANE Select	ENSP00000337443.3:n.361-71275A>C
ENST00000336868.7:c.361-71275A>C	ENSP00000337443.3:n.361-71275A>C
ENST00000571338.1:n.389+32310A>C
ENST00000575171.1:n.32-71275A>C
ENST00000577098.5:n.421+7800A>C
NM_022463.4:c.361-71275A>C	NP_071908.2:n.361-71275A>C
XM_005256756.3:c.361-71275A>C	XP_005256813.1:n.361-71275A>C
XM_005256756.4:c.361-71275A>C	XP_005256813.1:n.361-71275A>C
XM_005256758.3:c.-447A>C	XP_005256815.1:n.-447A>C
XM_017024949.1:c.361-71275A>C	XP_016880438.1:n.361-71275A>C
NM_022463.5:c.361-71275A>C MANE Select	NP_071908.2:n.361-71275A>C