Canonical Allele Identifier: CA286706572

Gene: NXN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.864155G>A , CM000679.2:g.864155G>A	GRCh38
NC_000017.10:g.767395G>A , CM000679.1:g.767395G>A	GRCh37
NC_000017.9:g.714145G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_022463.5:c.361-38077C>T MANE Select	NP_071908.2:n.361-38077C>T
ENST00000336868.8:c.361-38077C>T MANE Select	ENSP00000337443.3:n.361-38077C>T
NM_022463.4:c.361-38077C>T	NP_071908.2:n.361-38077C>T
ENST00000336868.7:c.361-38077C>T	ENSP00000337443.3:n.361-38077C>T
ENST00000571338.1:n.390-38077C>T
ENST00000575171.1:n.32-38077C>T
ENST00000575455.5:n.129+32731C>T
ENST00000577098.5:n.422-38077C>T
XM_005256756.3:c.361-38077C>T	XP_005256813.1:n.361-38077C>T
XM_005256756.4:c.361-38077C>T	XP_005256813.1:n.361-38077C>T
XM_005256758.2:c.21+32731C>T	XP_005256815.1:n.21+32731C>T
XM_005256758.3:c.21+32731C>T	XP_005256815.1:n.21+32731C>T
XM_017024949.1:c.361-38077C>T	XP_016880438.1:n.361-38077C>T