Canonical Allele Identifier: CA1829889563

Gene: CD274

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455436_5455437delinsCT , CM000671.2:g.5455436_5455437delinsCT	GRCh38
NC_000009.11:g.5455436_5455437delinsCT , CM000671.1:g.5455436_5455437delinsCT	GRCh37
NC_000009.10:g.5445436_5445437delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.-14-664_-14-663delinsCT MANE Select	ENSP00000370989.3:n.-14-664_-14-663delinsCT
ENST00000381573.8:c.-14-664_-14-663delinsCT	ENSP00000370985.4:n.-14-664_-14-663delinsCT
ENST00000381577.3:c.-14-664_-14-663delinsCT	ENSP00000370989.3:n.-14-664_-14-663delinsCT
NM_001267706.1:c.-14-664_-14-663delinsCT	NP_001254635.1:n.-14-664_-14-663delinsCT
NM_001314029.1:c.-14-664_-14-663delinsCT	NP_001300958.1:n.-14-664_-14-663delinsCT
NM_014143.3:c.-14-664_-14-663delinsCT	NP_054862.1:n.-14-664_-14-663delinsCT
NR_052005.1:n.95-664_95-663delinsCT
XM_006716759.2:c.-14-664_-14-663delinsCT	XP_006716822.1:n.-14-664_-14-663delinsCT
NM_014143.4:c.-14-664_-14-663delinsCT MANE Select	NP_054862.1:n.-14-664_-14-663delinsCT
NM_001314029.2:c.-14-664_-14-663delinsCT	NP_001300958.1:n.-14-664_-14-663delinsCT
NR_052005.2:n.56-664_56-663delinsCT
NM_001267706.2:c.-14-664_-14-663delinsCT	NP_001254635.1:n.-14-664_-14-663delinsCT