Canonical Allele Identifier: CA470405476

Gene: DLG5

Linked Data

• MyVariant Identifiers: chr10:g.79551553G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77791795G>C , CM000672.2:g.77791795G>C	GRCh38
NC_000010.10:g.79551553G>C , CM000672.1:g.79551553G>C	GRCh37
NC_000010.9:g.79221559G>C	NCBI36
NG_011484.1:g.139796C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372391.7:c.*645C>G MANE Select	ENSP00000361467.2:n.*645C>G
ENST00000372391.6:c.*645C>G	ENSP00000361467.2:n.*645C>G
ENST00000424842.5:c.3288C>G	ENSP00000394797.1:n.3288C>G
ENST00000475613.6:n.6242C>G
NM_004747.3:c.*645C>G	NP_004738.3:n.*645C>G
XM_005270276.3:c.*645C>G	XP_005270333.1:n.*645C>G
XM_006718056.2:c.*645C>G	XP_006718119.1:n.*645C>G
XM_011540341.1:c.*645C>G	XP_011538643.1:n.*645C>G
XM_011540342.1:c.*645C>G	XP_011538644.1:n.*645C>G
XM_011540343.1:c.*645C>G	XP_011538645.1:n.*645C>G
XM_011540344.1:c.*645C>G	XP_011538646.1:n.*645C>G
XM_011540345.1:c.*645C>G	XP_011538647.1:n.*645C>G
XM_011540347.1:c.*645C>G	XP_011538649.1:n.*645C>G
XM_005270276.4:c.*645C>G	XP_005270333.1:n.*645C>G
XM_006718056.3:c.*645C>G	XP_006718119.1:n.*645C>G
XM_011540341.3:c.*645C>G	XP_011538643.1:n.*645C>G
XM_011540344.2:c.*645C>G	XP_011538646.1:n.*645C>G
XM_011540347.2:c.*645C>G	XP_011538649.1:n.*645C>G
XM_017016913.1:c.*645C>G	XP_016872402.1:n.*645C>G
XM_017016914.1:c.*645C>G	XP_016872403.1:n.*645C>G
XM_017016915.1:c.*645C>G	XP_016872404.1:n.*645C>G
XM_024448250.1:c.*645C>G	XP_024304018.1:n.*645C>G
NM_004747.4:c.*645C>G MANE Select	NP_004738.3:n.*645C>G