Canonical Allele Identifier: CA2708733

Gene: NLGN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.174279363G>A , CM000665.2:g.174279363G>A	GRCh38
NC_000003.11:g.173997153G>A , CM000665.1:g.173997153G>A	GRCh37
NC_000003.10:g.175479847G>A	NCBI36
NG_046919.2:g.888465G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415045.2:c.1482G>A	ENSP00000410374.2:p.Lys494=
ENST00000695368.1:c.1422G>A MANE Select	ENSP00000511841.1:p.Lys474=
ENST00000361589.8:c.1362G>A	ENSP00000354541.4:p.Lys454=
ENST00000401917.4:c.717G>A	ENSP00000385750.4:p.Lys239=
ENST00000457714.5:c.1362G>A	ENSP00000392500.1:p.Lys454=
NM_014932.3:c.1362G>A	NP_055747.1:p.Lys454=
XM_005247232.1:c.1422G>A	XP_005247289.1:p.Lys474=
XM_005247233.1:c.1395G>A	XP_005247290.1:p.Lys465=
XM_005247234.1:c.1362G>A	XP_005247291.1:p.Lys454=
XM_005247235.2:c.1362G>A	XP_005247292.1:p.Lys454=
XM_005247236.1:c.1335G>A	XP_005247293.1:p.Lys445=
XM_005247237.2:c.906G>A	XP_005247294.1:p.Lys302=
XM_006713540.2:c.1422G>A	XP_006713603.1:p.Lys474=
XM_011512551.1:c.1422G>A	XP_011510853.1:p.Lys474=
XM_011512552.1:c.1422G>A	XP_011510854.1:p.Lys474=
XM_011512553.1:c.420G>A	XP_011510855.1:p.Lys140=
XM_011512554.1:c.420G>A	XP_011510856.1:p.Lys140=
XM_011512555.1:c.420G>A	XP_011510857.1:p.Lys140=
NM_001365923.1:c.1422G>A	NP_001352852.1:p.Lys474=
NM_001365924.1:c.1422G>A	NP_001352853.1:p.Lys474=
NM_001365925.1:c.1422G>A	NP_001352854.1:p.Lys474=
NM_001365926.1:c.1422G>A	NP_001352855.1:p.Lys474=
NM_001365927.1:c.1422G>A	NP_001352856.1:p.Lys474=
NM_001365928.1:c.1422G>A	NP_001352857.1:p.Lys474=
NM_001365929.1:c.1362G>A	NP_001352858.1:p.Lys454=
NM_001365930.1:c.1362G>A	NP_001352859.1:p.Lys454=
NM_001365931.1:c.1362G>A	NP_001352860.1:p.Lys454=
NM_001365932.1:c.1362G>A	NP_001352861.1:p.Lys454=
NM_001365933.1:c.1362G>A	NP_001352862.1:p.Lys454=
NM_001365934.1:c.1335G>A	NP_001352863.1:p.Lys445=
NM_001365935.1:c.1335G>A	NP_001352864.1:p.Lys445=
NM_001365936.1:c.1335G>A	NP_001352865.1:p.Lys445=
NM_014932.4:c.1362G>A	NP_055747.1:p.Lys454=
XM_005247237.3:c.906G>A	XP_005247294.1:p.Lys302=
XM_011512551.2:c.1422G>A	XP_011510853.1:p.Lys474=
XM_011512553.2:c.420G>A	XP_011510855.1:p.Lys140=
XM_011512554.2:c.420G>A	XP_011510856.1:p.Lys140=
XM_017005888.1:c.1422G>A	XP_016861377.1:p.Lys474=
XM_017005893.1:c.1422G>A	XP_016861382.1:p.Lys474=
XM_017005894.1:c.1422G>A	XP_016861383.1:p.Lys474=
XM_017005895.2:c.1422G>A	XP_016861384.1:p.Lys474=
XM_017005896.1:c.1422G>A	XP_016861385.1:p.Lys474=
XM_017005897.1:c.1395G>A	XP_016861386.1:p.Lys465=
XM_017005900.1:c.1362G>A	XP_016861389.1:p.Lys454=
XM_017005902.1:c.1335G>A	XP_016861391.1:p.Lys445=
NM_001365923.2:c.1422G>A	NP_001352852.1:p.Lys474=
NM_001365924.2:c.1422G>A	NP_001352853.1:p.Lys474=
NM_001365925.2:c.1422G>A MANE Select	NP_001352854.1:p.Lys474=
NM_001365926.2:c.1422G>A	NP_001352855.1:p.Lys474=
NM_001365927.2:c.1422G>A	NP_001352856.1:p.Lys474=
NM_001365928.2:c.1422G>A	NP_001352857.1:p.Lys474=
NM_001365929.2:c.1362G>A	NP_001352858.1:p.Lys454=
NM_001365930.2:c.1362G>A	NP_001352859.1:p.Lys454=
NM_001365931.2:c.1362G>A	NP_001352860.1:p.Lys454=
NM_001365932.2:c.1362G>A	NP_001352861.1:p.Lys454=
NM_001365933.2:c.1362G>A	NP_001352862.1:p.Lys454=
NM_001365934.2:c.1335G>A	NP_001352863.1:p.Lys445=
NM_001365935.2:c.1335G>A	NP_001352864.1:p.Lys445=
NM_001365936.2:c.1335G>A	NP_001352865.1:p.Lys445=
NM_014932.5:c.1362G>A	NP_055747.1:p.Lys454=