Canonical Allele Identifier: CA412012211

Gene: NLGN4X

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.5909240C>A , CM000685.2:g.5909240C>A	GRCh38
NC_000023.10:g.5827281C>A , CM000685.1:g.5827281C>A	GRCh37
NC_000023.9:g.5837281C>A	NCBI36
NG_008881.1:g.324426G>T
NG_008881.2:g.324643G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381095.8:c.626-1G>T MANE Select	ENSP00000370485.3:n.626-1G>T
ENST00000538097.6:c.686-1G>T	ENSP00000439203.3:n.686-1G>T
ENST00000275857.10:c.626-1G>T	ENSP00000275857.6:n.626-1G>T
ENST00000381092.1:c.626-1G>T	ENSP00000370482.1:n.626-1G>T
ENST00000381093.6:c.626-1G>T	ENSP00000370483.3:n.626-1G>T
ENST00000381095.7:c.626-1G>T	ENSP00000370485.3:n.626-1G>T
ENST00000538097.5:c.629-1G>T	ENSP00000439203.2:n.629-1G>T
NM_001282145.1:c.626-1G>T	NP_001269074.1:n.626-1G>T
NM_001282146.1:c.626-1G>T	NP_001269075.1:n.626-1G>T
NM_020742.3:c.626-1G>T	NP_065793.1:n.626-1G>T
NM_181332.2:c.626-1G>T	NP_851849.1:n.626-1G>T
XM_005274564.1:c.686-1G>T	XP_005274621.1:n.686-1G>T
XM_005274565.1:c.686-1G>T	XP_005274622.1:n.686-1G>T
XM_005274566.3:c.686-1G>T	XP_005274623.1:n.686-1G>T
XM_006724504.2:c.686-1G>T	XP_006724567.1:n.686-1G>T
XM_011545547.1:c.686-1G>T	XP_011543849.1:n.686-1G>T
XM_011545548.1:c.686-1G>T	XP_011543850.1:n.686-1G>T
XM_005274564.3:c.686-1G>T	XP_005274621.1:n.686-1G>T
XM_005274565.2:c.686-1G>T	XP_005274622.1:n.686-1G>T
XM_005274566.4:c.686-1G>T	XP_005274623.1:n.686-1G>T
XM_006724504.3:c.686-1G>T	XP_006724567.1:n.686-1G>T
XM_011545547.2:c.686-1G>T	XP_011543849.1:n.686-1G>T
XM_011545548.2:c.686-1G>T	XP_011543850.1:n.686-1G>T
XM_017029691.1:c.626-1G>T	XP_016885180.1:n.626-1G>T
XM_017029692.1:c.626-1G>T	XP_016885181.1:n.626-1G>T
XM_017029693.1:c.626-1G>T	XP_016885182.1:n.626-1G>T
NM_181332.3:c.626-1G>T MANE Select	NP_851849.1:n.626-1G>T
NM_001282145.2:c.626-1G>T	NP_001269074.1:n.626-1G>T
NM_001282146.2:c.626-1G>T	NP_001269075.1:n.626-1G>T
NM_020742.4:c.626-1G>T	NP_065793.1:n.626-1G>T