Canonical Allele Identifier: CA1120803323

Gene: CD274

Linked Data

• dbSNP Id: rs1819285908
• gnomAD v3: 9-5455532-A-AG
• gnomAD v4: 9-5455532-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455532_5455533insG , CM000671.2:g.5455532_5455533insG	GRCh38
NC_000009.11:g.5455532_5455533insG , CM000671.1:g.5455532_5455533insG	GRCh37
NC_000009.10:g.5445532_5445533insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.-14-568_-14-567insG MANE Select	ENSP00000370989.3:n.-14-568_-14-567insG
ENST00000381573.8:c.-14-568_-14-567insG	ENSP00000370985.4:n.-14-568_-14-567insG
ENST00000381577.3:c.-14-568_-14-567insG	ENSP00000370989.3:n.-14-568_-14-567insG
NM_001267706.1:c.-14-568_-14-567insG	NP_001254635.1:n.-14-568_-14-567insG
NM_001314029.1:c.-14-568_-14-567insG	NP_001300958.1:n.-14-568_-14-567insG
NM_014143.3:c.-14-568_-14-567insG	NP_054862.1:n.-14-568_-14-567insG
NR_052005.1:n.95-568_95-567insG
XM_006716759.2:c.-14-568_-14-567insG	XP_006716822.1:n.-14-568_-14-567insG
NM_014143.4:c.-14-568_-14-567insG MANE Select	NP_054862.1:n.-14-568_-14-567insG
NM_001314029.2:c.-14-568_-14-567insG	NP_001300958.1:n.-14-568_-14-567insG
NR_052005.2:n.56-568_56-567insG
NM_001267706.2:c.-14-568_-14-567insG	NP_001254635.1:n.-14-568_-14-567insG