Canonical Allele Identifier: CA188503849

Gene: CD274

Linked Data

• dbSNP Id: rs564509591
• gnomAD v2: 9-5455833-TG-T
• gnomAD v3: 9-5455833-TG-T
• gnomAD v4: 9-5455833-TG-T
• MyVariant Identifiers: chr9:g.5455834del (hg19) ; chr9:g.5455834del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455836del , CM000671.2:g.5455836del	GRCh38
NC_000009.11:g.5455836del , CM000671.1:g.5455836del	GRCh37
NC_000009.10:g.5445836del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381577.4:c.-14-264del MANE Select	ENSP00000370989.3:n.-14-264del
ENST00000381573.8:c.-14-264del	ENSP00000370985.4:n.-14-264del
ENST00000381577.3:c.-14-264del	ENSP00000370989.3:n.-14-264del
NM_001267706.1:c.-14-264del	NP_001254635.1:n.-14-264del
NM_001314029.1:c.-14-264del	NP_001300958.1:n.-14-264del
NM_014143.3:c.-14-264del	NP_054862.1:n.-14-264del
NR_052005.1:n.95-264del
XM_006716759.2:c.-14-264del	XP_006716822.1:n.-14-264del
NM_014143.4:c.-14-264del MANE Select	NP_054862.1:n.-14-264del
NM_001314029.2:c.-14-264del	NP_001300958.1:n.-14-264del
NR_052005.2:n.56-264del
NM_001267706.2:c.-14-264del	NP_001254635.1:n.-14-264del