Canonical Allele Identifier: CA1921414372

Gene: DLG5

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77791783G= , CM000672.2:g.77791783G=	GRCh38
NC_000010.10:g.79551541G= , CM000672.1:g.79551541G=	GRCh37
NC_000010.9:g.79221547G=	NCBI36
NG_011484.1:g.139808C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372391.7:c.*657C= MANE Select	ENSP00000361467.2:n.*657C=
ENST00000372391.6:c.*657C=	ENSP00000361467.2:n.*657C=
ENST00000424842.5:c.3300C=	ENSP00000394797.1:n.3300C=
ENST00000475613.6:n.6254C=
NM_004747.3:c.*657C=	NP_004738.3:n.*657C=
XM_005270276.3:c.*657C=	XP_005270333.1:n.*657C=
XM_006718056.2:c.*657C=	XP_006718119.1:n.*657C=
XM_011540341.1:c.*657C=	XP_011538643.1:n.*657C=
XM_011540342.1:c.*657C=	XP_011538644.1:n.*657C=
XM_011540343.1:c.*657C=	XP_011538645.1:n.*657C=
XM_011540344.1:c.*657C=	XP_011538646.1:n.*657C=
XM_011540345.1:c.*657C=	XP_011538647.1:n.*657C=
XM_011540347.1:c.*657C=	XP_011538649.1:n.*657C=
XM_005270276.4:c.*657C=	XP_005270333.1:n.*657C=
XM_006718056.3:c.*657C=	XP_006718119.1:n.*657C=
XM_011540341.3:c.*657C=	XP_011538643.1:n.*657C=
XM_011540344.2:c.*657C=	XP_011538646.1:n.*657C=
XM_011540347.2:c.*657C=	XP_011538649.1:n.*657C=
XM_017016913.1:c.*657C=	XP_016872402.1:n.*657C=
XM_017016914.1:c.*657C=	XP_016872403.1:n.*657C=
XM_017016915.1:c.*657C=	XP_016872404.1:n.*657C=
XM_024448250.1:c.*657C=	XP_024304018.1:n.*657C=
NM_004747.4:c.*657C= MANE Select	NP_004738.3:n.*657C=