Canonical Allele Identifier: CA209786369

Gene: DLG5

Linked Data

• dbSNP Id: rs372244596
• gnomAD v2: 10-79551548-A-G
• gnomAD v3: 10-77791790-A-G
• gnomAD v4: 10-77791790-A-G
• MyVariant Identifiers: chr10:g.79551548A>G (hg19) ; chr10:g.77791790A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77791790A>G , CM000672.2:g.77791790A>G	GRCh38
NC_000010.10:g.79551548A>G , CM000672.1:g.79551548A>G	GRCh37
NC_000010.9:g.79221554A>G	NCBI36
NG_011484.1:g.139801T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372391.7:c.*650T>C MANE Select	ENSP00000361467.2:n.*650T>C
ENST00000372391.6:c.*650T>C	ENSP00000361467.2:n.*650T>C
ENST00000424842.5:c.3293T>C	ENSP00000394797.1:n.3293T>C
ENST00000475613.6:n.6247T>C
NM_004747.3:c.*650T>C	NP_004738.3:n.*650T>C
XM_005270276.3:c.*650T>C	XP_005270333.1:n.*650T>C
XM_006718056.2:c.*650T>C	XP_006718119.1:n.*650T>C
XM_011540341.1:c.*650T>C	XP_011538643.1:n.*650T>C
XM_011540342.1:c.*650T>C	XP_011538644.1:n.*650T>C
XM_011540343.1:c.*650T>C	XP_011538645.1:n.*650T>C
XM_011540344.1:c.*650T>C	XP_011538646.1:n.*650T>C
XM_011540345.1:c.*650T>C	XP_011538647.1:n.*650T>C
XM_011540347.1:c.*650T>C	XP_011538649.1:n.*650T>C
XM_005270276.4:c.*650T>C	XP_005270333.1:n.*650T>C
XM_006718056.3:c.*650T>C	XP_006718119.1:n.*650T>C
XM_011540341.3:c.*650T>C	XP_011538643.1:n.*650T>C
XM_011540344.2:c.*650T>C	XP_011538646.1:n.*650T>C
XM_011540347.2:c.*650T>C	XP_011538649.1:n.*650T>C
XM_017016913.1:c.*650T>C	XP_016872402.1:n.*650T>C
XM_017016914.1:c.*650T>C	XP_016872403.1:n.*650T>C
XM_017016915.1:c.*650T>C	XP_016872404.1:n.*650T>C
XM_024448250.1:c.*650T>C	XP_024304018.1:n.*650T>C
NM_004747.4:c.*650T>C MANE Select	NP_004738.3:n.*650T>C