Canonical Allele Identifier: CA1105646223
Gene: DLD HGNC NCBI

Linked Data

gnomAD v3: 7-107920238-T-TTCCTCA
gnomAD v4: 7-107920238-T-TTCCTCA
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920238_107920239insTCCTCA , CM000669.2:g.107920238_107920239insTCCTCA GRCh38
NC_000007.13:g.107560683_107560684insTCCTCA , CM000669.1:g.107560683_107560684insTCCTCA GRCh37
NC_000007.12:g.107347919_107347920insTCCTCA NCBI36
NG_008045.1:g.34098_34099insTCCTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*979_*980insTCCTCA MANE Select ENSP00000205402.3:n.*979_*980insTCCTCA
ENST00000205402.9:c.*979_*980insTCCTCA ENSP00000205402.3:n.*979_*980insTCCTCA
ENST00000417551.5:c.*124+855_*124+856insTCCTCA ENSP00000390667.1:n.*124+855_*124+856insTCCTCA
NM_000108.4:c.*979_*980insTCCTCA NP_000099.2:n.*979_*980insTCCTCA
NM_001289750.1:c.*979_*980insTCCTCA NP_001276679.1:n.*979_*980insTCCTCA
NM_001289751.1:c.*979_*980insTCCTCA NP_001276680.1:n.*979_*980insTCCTCA
NM_001289752.1:c.*979_*980insTCCTCA NP_001276681.1:n.*979_*980insTCCTCA
NM_000108.5:c.*979_*980insTCCTCA MANE Select NP_000099.2:n.*979_*980insTCCTCA
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