Canonical Allele Identifier: CA1829889772

Gene: CD274

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455658A= , CM000671.2:g.5455658A=	GRCh38
NC_000009.11:g.5455658A= , CM000671.1:g.5455658A=	GRCh37
NC_000009.10:g.5445658A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381577.4:c.-14-442A= MANE Select	ENSP00000370989.3:n.-14-442A=
ENST00000381573.8:c.-14-442A=	ENSP00000370985.4:n.-14-442A=
ENST00000381577.3:c.-14-442A=	ENSP00000370989.3:n.-14-442A=
NM_001267706.1:c.-14-442A=	NP_001254635.1:n.-14-442A=
NM_001314029.1:c.-14-442A=	NP_001300958.1:n.-14-442A=
NM_014143.3:c.-14-442A=	NP_054862.1:n.-14-442A=
NR_052005.1:n.95-442A=
XM_006716759.2:c.-14-442A=	XP_006716822.1:n.-14-442A=
NM_014143.4:c.-14-442A= MANE Select	NP_054862.1:n.-14-442A=
NM_001314029.2:c.-14-442A=	NP_001300958.1:n.-14-442A=
NR_052005.2:n.56-442A=
NM_001267706.2:c.-14-442A=	NP_001254635.1:n.-14-442A=