Canonical Allele Identifier: CA1921443180

Gene: DLG5

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77856847T= , CM000672.2:g.77856847T=	GRCh38
NC_000010.10:g.79616605T= , CM000672.1:g.79616605T=	GRCh37
NC_000010.9:g.79286611T=	NCBI36
NG_011484.1:g.74744A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004747.4:c.419A= MANE Select	NP_004738.3:p.Gln140=
ENST00000372391.7:c.419A= MANE Select	ENSP00000361467.2:p.Gln140=
NM_004747.3:c.419A=	NP_004738.3:p.Gln140=
ENST00000372391.6:c.419A=	ENSP00000361467.2:p.Gln140=
ENST00000468332.6:c.194A=	ENSP00000473298.1:p.Gln65=
ENST00000475613.6:n.93+12252A=
XM_005270276.3:c.419A=	XP_005270333.1:p.Gln140=
XM_005270276.4:c.419A=	XP_005270333.1:p.Gln140=
XM_006718056.2:c.419A=	XP_006718119.1:p.Gln140=
XM_006718056.3:c.419A=	XP_006718119.1:p.Gln140=
XM_006718057.2:c.419A=	XP_006718120.1:p.Gln140=
XM_006718057.3:c.419A=	XP_006718120.1:p.Gln140=
XM_011540341.1:c.242A=	XP_011538643.1:p.Gln81=
XM_011540341.3:c.242A=	XP_011538643.1:p.Gln81=
XM_011540342.1:c.149A=	XP_011538644.1:p.Gln50=
XM_011540343.1:c.89A=	XP_011538645.1:p.Gln30=
XM_011540344.1:c.83A=	XP_011538646.1:p.Gln28=
XM_011540344.2:c.83A=	XP_011538646.1:p.Gln28=
XM_011540345.1:c.-47A=	XP_011538647.1:n.-47A=
XM_011540346.1:c.419A=	XP_011538648.1:p.Gln140=
XM_011540346.2:c.419A=	XP_011538648.1:p.Gln140=
XM_017016913.1:c.137A=	XP_016872402.1:p.Gln46=
XM_017016914.1:c.89A=	XP_016872403.1:p.Gln30=
XR_945874.1:n.450A=
XR_945874.2:n.461A=