Canonical Allele Identifier: CA2638666194
Gene: DLX4 HGNC NCBI

Linked Data

gnomAD v4: 17-49974016-T-TCCA
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974016_49974017insCCA , CM000679.2:g.49974016_49974017insCCA GRCh38
NC_000017.10:g.48051380_48051381insCCA , CM000679.1:g.48051380_48051381insCCA GRCh37
NC_000017.9:g.45406379_45406380insCCA NCBI36
NG_030592.1:g.9819_9820insCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1677_1678insCCA
ENST00000240306.5:c.*73_*74insCCA MANE Select ENSP00000240306.3:n.*73_*74insCCA
ENST00000240306.4:c.*73_*74insCCA ENSP00000240306.3:n.*73_*74insCCA
ENST00000411890.3:c.*73_*74insCCA ENSP00000410622.2:n.*73_*74insCCA
ENST00000611342.1:c.*666_*667insCCA ENSP00000480366.1:n.*666_*667insCCA
NM_001934.3:c.*73_*74insCCA NP_001925.2:n.*73_*74insCCA
NM_138281.2:c.*73_*74insCCA NP_612138.1:n.*73_*74insCCA
XM_011524459.1:c.*73_*74insCCA XP_011522761.1:n.*73_*74insCCA
XM_017024291.1:c.*73_*74insCCA XP_016879780.1:n.*73_*74insCCA
NM_138281.3:c.*73_*74insCCA MANE Select NP_612138.1:n.*73_*74insCCA
NM_001934.4:c.*73_*74insCCA NP_001925.2:n.*73_*74insCCA
Search 100 bp 5'
Search 100 bp 3'