Canonical Allele Identifier: CA1987925705

Gene: DLG2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.85111277G>T , CM000673.2:g.85111277G>T	GRCh38
NC_000011.9:g.84822321G>T , CM000673.1:g.84822321G>T	GRCh37
NC_000011.8:g.84499969G>T	NCBI36
NG_021375.1:g.520994C>A
NG_021375.2:g.522259C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527088.2:c.105+384C>A	ENSP00000435809.2:n.105+384C>A
ENST00000705960.1:n.714+384C>A
ENST00000706006.1:c.468+384C>A	ENSP00000516200.1:n.468+384C>A
ENST00000706007.1:c.*271+43279C>A	ENSP00000516201.1:n.*271+43279C>A
ENST00000706226.1:c.393+43279C>A	ENSP00000516284.1:n.393+43279C>A
ENST00000706233.1:c.393+43279C>A	ENSP00000516288.1:n.393+43279C>A
ENST00000376104.7:c.357+384C>A MANE Select	ENSP00000365272.2:n.357+384C>A
ENST00000650630.1:c.468+384C>A	ENSP00000497771.1:n.468+384C>A
ENST00000376104.6:c.357+384C>A	ENSP00000365272.2:n.357+384C>A
ENST00000527088.1:c.105+384C>A	ENSP00000435809.1:n.105+384C>A
NM_001142699.1:c.357+384C>A	NP_001136171.1:n.357+384C>A
XM_011544778.1:c.507+384C>A	XP_011543080.1:n.507+384C>A
XM_011544779.1:c.468+384C>A	XP_011543081.1:n.468+384C>A
XM_011544780.1:c.507+384C>A	XP_011543082.1:n.507+384C>A
XM_011544781.1:c.432+43279C>A	XP_011543083.1:n.432+43279C>A
XM_011544782.1:c.105+384C>A	XP_011543084.1:n.105+384C>A
XM_011544785.1:c.30+21491C>A	XP_011543087.1:n.30+21491C>A
XM_011544786.1:c.507+384C>A	XP_011543088.1:n.507+384C>A
NM_001351274.1:c.393+43279C>A	NP_001338203.1:n.393+43279C>A
NM_001351275.1:c.393+43279C>A	NP_001338204.1:n.393+43279C>A
XM_011544778.3:c.507+384C>A	XP_011543080.1:n.507+384C>A
XM_011544780.3:c.507+384C>A	XP_011543082.1:n.507+384C>A
XM_011544782.2:c.105+384C>A	XP_011543084.1:n.105+384C>A
XM_017017254.2:c.507+384C>A	XP_016872743.1:n.507+384C>A
XM_017017255.2:c.468+384C>A	XP_016872744.1:n.468+384C>A
XM_017017256.2:c.468+384C>A	XP_016872745.1:n.468+384C>A
XM_017017257.2:c.468+384C>A	XP_016872746.1:n.468+384C>A
XM_017017258.1:c.345+384C>A	XP_016872747.1:n.345+384C>A
XM_017017261.2:c.507+384C>A	XP_016872750.1:n.507+384C>A
XM_017017263.1:c.105+384C>A	XP_016872752.1:n.105+384C>A
XM_017017269.1:c.30+21491C>A	XP_016872758.1:n.30+21491C>A
XM_017017270.1:c.105+384C>A	XP_016872759.1:n.105+384C>A
XM_017017276.1:c.30+21491C>A	XP_016872765.1:n.30+21491C>A
XM_017017279.1:c.105+384C>A	XP_016872768.1:n.105+384C>A
XM_017017280.2:c.105+384C>A	XP_016872769.1:n.105+384C>A
XM_017017285.1:c.30+21491C>A	XP_016872774.1:n.30+21491C>A
XM_024448378.1:c.393+43279C>A	XP_024304146.1:n.393+43279C>A
XM_024448379.1:c.393+43279C>A	XP_024304147.1:n.393+43279C>A
NM_001351274.2:c.393+43279C>A	NP_001338203.1:n.393+43279C>A
NM_001142699.3:c.357+384C>A MANE Select	NP_001136171.1:n.357+384C>A
NM_001351275.2:c.393+43279C>A	NP_001338204.1:n.393+43279C>A