Canonical Allele Identifier: CA902760123

Gene: NLGN1

Linked Data

• dbSNP Id: rs1348232149
• MyVariant Identifiers: chr3:g.173453924A>G (hg19) ; chr3:g.173736134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173736134A>G , CM000665.2:g.173736134A>G	GRCh38
NC_000003.11:g.173453924A>G , CM000665.1:g.173453924A>G	GRCh37
NC_000003.10:g.174936618A>G	NCBI36
NG_046919.2:g.345236A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415045.2:c.554-64159A>G	ENSP00000410374.2:n.554-64159A>G
ENST00000695368.1:c.554-71546A>G MANE Select	ENSP00000511841.1:n.554-71546A>G
ENST00000361589.8:c.494-71546A>G	ENSP00000354541.4:n.494-71546A>G
ENST00000415045.1:c.554-64159A>G	ENSP00000410374.1:n.554-64159A>G
ENST00000457714.5:c.494-71546A>G	ENSP00000392500.1:n.494-71546A>G
NM_014932.3:c.494-71546A>G	NP_055747.1:n.494-71546A>G
XM_005247232.1:c.494-64159A>G	XP_005247289.1:n.494-64159A>G
XM_005247233.1:c.494-64159A>G	XP_005247290.1:n.494-64159A>G
XM_005247234.1:c.494-71546A>G	XP_005247291.1:n.494-71546A>G
XM_005247235.2:c.494-71546A>G	XP_005247292.1:n.494-71546A>G
XM_005247236.1:c.494-71546A>G	XP_005247293.1:n.494-71546A>G
XM_005247237.2:c.37+50343A>G	XP_005247294.1:n.37+50343A>G
XM_006713540.2:c.494-64159A>G	XP_006713603.1:n.494-64159A>G
XM_011512551.1:c.494-64159A>G	XP_011510853.1:n.494-64159A>G
XM_011512552.1:c.494-64159A>G	XP_011510854.1:n.494-64159A>G
NM_001365923.1:c.494-64159A>G	NP_001352852.1:n.494-64159A>G
NM_001365924.1:c.554-71546A>G	NP_001352853.1:n.554-71546A>G
NM_001365925.1:c.554-71546A>G	NP_001352854.1:n.554-71546A>G
NM_001365926.1:c.554-71546A>G	NP_001352855.1:n.554-71546A>G
NM_001365927.1:c.494-64159A>G	NP_001352856.1:n.494-64159A>G
NM_001365928.1:c.554-71546A>G	NP_001352857.1:n.554-71546A>G
NM_001365929.1:c.494-71546A>G	NP_001352858.1:n.494-71546A>G
NM_001365930.1:c.494-71546A>G	NP_001352859.1:n.494-71546A>G
NM_001365931.1:c.494-71546A>G	NP_001352860.1:n.494-71546A>G
NM_001365932.1:c.494-71546A>G	NP_001352861.1:n.494-71546A>G
NM_001365933.1:c.494-71546A>G	NP_001352862.1:n.494-71546A>G
NM_001365934.1:c.494-71546A>G	NP_001352863.1:n.494-71546A>G
NM_001365935.1:c.494-71546A>G	NP_001352864.1:n.494-71546A>G
NM_001365936.1:c.494-71546A>G	NP_001352865.1:n.494-71546A>G
NM_014932.4:c.494-71546A>G	NP_055747.1:n.494-71546A>G
XM_005247237.3:c.37+50343A>G	XP_005247294.1:n.37+50343A>G
XM_011512551.2:c.494-64159A>G	XP_011510853.1:n.494-64159A>G
XM_017005888.1:c.494-64159A>G	XP_016861377.1:n.494-64159A>G
XM_017005893.1:c.494-64159A>G	XP_016861382.1:n.494-64159A>G
XM_017005894.1:c.494-64159A>G	XP_016861383.1:n.494-64159A>G
XM_017005895.2:c.494-64159A>G	XP_016861384.1:n.494-64159A>G
XM_017005896.1:c.494-64159A>G	XP_016861385.1:n.494-64159A>G
XM_017005897.1:c.494-64159A>G	XP_016861386.1:n.494-64159A>G
XM_017005900.1:c.494-71546A>G	XP_016861389.1:n.494-71546A>G
XM_017005902.1:c.494-71546A>G	XP_016861391.1:n.494-71546A>G
XR_924728.3:n.2086T>C
NM_001365923.2:c.494-64159A>G	NP_001352852.1:n.494-64159A>G
NM_001365924.2:c.554-71546A>G	NP_001352853.1:n.554-71546A>G
NM_001365925.2:c.554-71546A>G MANE Select	NP_001352854.1:n.554-71546A>G
NM_001365926.2:c.554-71546A>G	NP_001352855.1:n.554-71546A>G
NM_001365927.2:c.494-64159A>G	NP_001352856.1:n.494-64159A>G
NM_001365928.2:c.554-71546A>G	NP_001352857.1:n.554-71546A>G
NM_001365929.2:c.494-71546A>G	NP_001352858.1:n.494-71546A>G
NM_001365930.2:c.494-71546A>G	NP_001352859.1:n.494-71546A>G
NM_001365931.2:c.494-71546A>G	NP_001352860.1:n.494-71546A>G
NM_001365932.2:c.494-71546A>G	NP_001352861.1:n.494-71546A>G
NM_001365933.2:c.494-71546A>G	NP_001352862.1:n.494-71546A>G
NM_001365934.2:c.494-71546A>G	NP_001352863.1:n.494-71546A>G
NM_001365935.2:c.494-71546A>G	NP_001352864.1:n.494-71546A>G
NM_001365936.2:c.494-71546A>G	NP_001352865.1:n.494-71546A>G
NM_014932.5:c.494-71546A>G	NP_055747.1:n.494-71546A>G