Canonical Allele Identifier: CA2689322348
Gene: CD274 HGNC NCBI

Linked Data

gnomAD v4: 9-5468211-C-CAGA
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5468213_5468214insAAG , CM000671.2:g.5468213_5468214insAAG GRCh38
NC_000009.11:g.5468213_5468214insAAG , CM000671.1:g.5468213_5468214insAAG GRCh37
NC_000009.10:g.5458213_5458214insAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381577.4:c.*351_*352insAAG MANE Select ENSP00000370989.3:n.*351_*352insAAG
ENST00000381573.8:c.*351_*352insAAG ENSP00000370985.4:n.*351_*352insAAG
ENST00000381577.3:c.*351_*352insAAG ENSP00000370989.3:n.*351_*352insAAG
NM_001267706.1:c.*351_*352insAAG NP_001254635.1:n.*351_*352insAAG
NM_014143.3:c.*351_*352insAAG NP_054862.1:n.*351_*352insAAG
NR_052005.1:n.1159_1160insAAG
NM_014143.4:c.*351_*352insAAG MANE Select NP_054862.1:n.*351_*352insAAG
NR_052005.2:n.1120_1121insAAG
NM_001267706.2:c.*351_*352insAAG NP_001254635.1:n.*351_*352insAAG
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