Canonical Allele Identifier: CA1120803369
Gene: CD274 HGNC NCBI

Linked Data

dbSNP Id: rs1819288479
gnomAD v3: 9-5455671-TA-T
gnomAD v4: 9-5455671-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5455672del , CM000671.2:g.5455672del GRCh38
NC_000009.11:g.5455672del , CM000671.1:g.5455672del GRCh37
NC_000009.10:g.5445672del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.-14-428del MANE Select ENSP00000370989.3:n.-14-428del
ENST00000381573.8:c.-14-428del ENSP00000370985.4:n.-14-428del
ENST00000381577.3:c.-14-428del ENSP00000370989.3:n.-14-428del
NM_001267706.1:c.-14-428del NP_001254635.1:n.-14-428del
NM_001314029.1:c.-14-428del NP_001300958.1:n.-14-428del
NM_014143.3:c.-14-428del NP_054862.1:n.-14-428del
NR_052005.1:n.95-428del
XM_006716759.2:c.-14-428del XP_006716822.1:n.-14-428del
NM_014143.4:c.-14-428del MANE Select NP_054862.1:n.-14-428del
NM_001314029.2:c.-14-428del NP_001300958.1:n.-14-428del
NR_052005.2:n.56-428del
NM_001267706.2:c.-14-428del NP_001254635.1:n.-14-428del
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