Canonical Allele Identifier: CA1921427445

Gene: DLG5

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77821218G= , CM000672.2:g.77821218G=	GRCh38
NC_000010.10:g.79580976G= , CM000672.1:g.79580976G=	GRCh37
NC_000010.9:g.79250982G=	NCBI36
NG_011484.1:g.110373C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004747.4:c.3266C= MANE Select	NP_004738.3:p.Pro1089=
ENST00000372391.7:c.3266C= MANE Select	ENSP00000361467.2:p.Pro1089=
NM_004747.3:c.3266C=	NP_004738.3:p.Pro1089=
ENST00000372391.6:c.3266C=	ENSP00000361467.2:p.Pro1089=
ENST00000424842.5:c.286-1200C=	ENSP00000394797.1:n.286-1200C=
ENST00000459739.5:n.321C=
ENST00000468332.6:c.3268C=	ENSP00000473298.1:n.3268C=
ENST00000475613.6:n.1611C=
XM_005270276.3:c.3254C=	XP_005270333.1:p.Pro1085=
XM_005270276.4:c.3254C=	XP_005270333.1:p.Pro1085=
XM_006718056.2:c.2383-1200C=	XP_006718119.1:n.2383-1200C=
XM_006718056.3:c.2383-1200C=	XP_006718119.1:n.2383-1200C=
XM_006718057.2:c.3266C=	XP_006718120.1:p.Pro1089=
XM_006718057.3:c.3266C=	XP_006718120.1:p.Pro1089=
XM_011540341.1:c.3089C=	XP_011538643.1:p.Pro1030=
XM_011540341.3:c.3089C=	XP_011538643.1:p.Pro1030=
XM_011540342.1:c.2996C=	XP_011538644.1:p.Pro999=
XM_011540343.1:c.2936C=	XP_011538645.1:p.Pro979=
XM_011540344.1:c.2930C=	XP_011538646.1:p.Pro977=
XM_011540344.2:c.2930C=	XP_011538646.1:p.Pro977=
XM_011540345.1:c.2801C=	XP_011538647.1:p.Pro934=
XM_011540346.1:c.3266C=	XP_011538648.1:p.Pro1089=
XM_011540346.2:c.3266C=	XP_011538648.1:p.Pro1089=
XM_011540347.1:c.2348C=	XP_011538649.1:p.Pro783=
XM_011540347.2:c.2348C=	XP_011538649.1:p.Pro783=
XM_017016913.1:c.2984C=	XP_016872402.1:p.Pro995=
XM_017016914.1:c.2936C=	XP_016872403.1:p.Pro979=
XM_017016915.1:c.2348C=	XP_016872404.1:p.Pro783=
XM_024448250.1:c.1811C=	XP_024304018.1:p.Pro604=
XR_945874.1:n.3297C=
XR_945874.2:n.3308C=