Canonical Allele Identifier: CA412015581

Gene: NLGN4X

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.6151417A>G , CM000685.2:g.6151417A>G	GRCh38
NC_000023.10:g.6069458A>G , CM000685.1:g.6069458A>G	GRCh37
NC_000023.9:g.6079458A>G	NCBI36
NG_008881.1:g.82249T>C
NG_008881.2:g.82466T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181332.3:c.50T>C MANE Select	NP_851849.1:p.Val17Ala
ENST00000381095.8:c.50T>C MANE Select	ENSP00000370485.3:p.Val17Ala
NM_001282145.1:c.50T>C	NP_001269074.1:p.Val17Ala
NM_001282145.2:c.50T>C	NP_001269074.1:p.Val17Ala
NM_001282146.1:c.50T>C	NP_001269075.1:p.Val17Ala
NM_001282146.2:c.50T>C	NP_001269075.1:p.Val17Ala
NM_020742.3:c.50T>C	NP_065793.1:p.Val17Ala
NM_020742.4:c.50T>C	NP_065793.1:p.Val17Ala
NM_181332.2:c.50T>C	NP_851849.1:p.Val17Ala
ENST00000275857.10:c.50T>C	ENSP00000275857.6:p.Val17Ala
ENST00000381092.1:c.50T>C	ENSP00000370482.1:p.Val17Ala
ENST00000381093.6:c.50T>C	ENSP00000370483.3:p.Val17Ala
ENST00000381095.7:c.50T>C	ENSP00000370485.3:p.Val17Ala
ENST00000469740.1:n.486T>C
ENST00000483337.1:n.622T>C
ENST00000538097.5:c.-8T>C	ENSP00000439203.2:n.-8T>C
ENST00000538097.6:c.50T>C	ENSP00000439203.3:p.Val17Ala
XM_005274564.1:c.50T>C	XP_005274621.1:p.Val17Ala
XM_005274564.3:c.50T>C	XP_005274621.1:p.Val17Ala
XM_005274565.1:c.50T>C	XP_005274622.1:p.Val17Ala
XM_005274565.2:c.50T>C	XP_005274622.1:p.Val17Ala
XM_005274566.3:c.50T>C	XP_005274623.1:p.Val17Ala
XM_005274566.4:c.50T>C	XP_005274623.1:p.Val17Ala
XM_006724504.2:c.50T>C	XP_006724567.1:p.Val17Ala
XM_006724504.3:c.50T>C	XP_006724567.1:p.Val17Ala
XM_011545547.1:c.50T>C	XP_011543849.1:p.Val17Ala
XM_011545547.2:c.50T>C	XP_011543849.1:p.Val17Ala
XM_011545548.1:c.50T>C	XP_011543850.1:p.Val17Ala
XM_011545548.2:c.50T>C	XP_011543850.1:p.Val17Ala
XM_017029691.1:c.50T>C	XP_016885180.1:p.Val17Ala
XM_017029692.1:c.50T>C	XP_016885181.1:p.Val17Ala
XM_017029693.1:c.50T>C	XP_016885182.1:p.Val17Ala