Canonical Allele Identifier: CA14496066
Gene: DLG4 HGNC NCBI

Linked Data

dbSNP Id: rs314253
gnomAD v2: 17-7091650-T-C
gnomAD v3: 17-7188331-T-C
gnomAD v4: 17-7188331-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7188331T>C , CM000679.2:g.7188331T>C GRCh38
NC_000017.10:g.7091650T>C , CM000679.1:g.7091650T>C GRCh37
NC_000017.9:g.7032374T>C NCBI36
NG_008391.2:g.36720A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399506.9:c.*2377A>G MANE Select ENSP00000382425.2:n.*2377A>G
NM_001128827.3:c.*2377A>G NP_001122299.1:n.*2377A>G
NM_001321075.3:c.*2377A>G MANE Select NP_001308004.1:n.*2377A>G
NM_001321076.2:c.*2377A>G NP_001308005.1:n.*2377A>G
NM_001321077.2:c.*2377A>G NP_001308006.1:n.*2377A>G
NM_001369566.2:c.*2377A>G NP_001356495.1:n.*2377A>G
NM_001128827.4:c.*2377A>G NP_001122299.1:n.*2377A>G
NM_001321076.3:c.*2377A>G NP_001308005.1:n.*2377A>G
NM_001321077.3:c.*2377A>G NP_001308006.1:n.*2377A>G
NM_001369566.3:c.*2377A>G NP_001356495.1:n.*2377A>G