Canonical Allele Identifier: CA1829889924

Gene: CD274

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455833_5455834delinsTG , CM000671.2:g.5455833_5455834delinsTG	GRCh38
NC_000009.11:g.5455833_5455834delinsTG , CM000671.1:g.5455833_5455834delinsTG	GRCh37
NC_000009.10:g.5445833_5445834delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.-14-267_-14-266delinsTG MANE Select	ENSP00000370989.3:n.-14-267_-14-266delinsTG
ENST00000381573.8:c.-14-267_-14-266delinsTG	ENSP00000370985.4:n.-14-267_-14-266delinsTG
ENST00000381577.3:c.-14-267_-14-266delinsTG	ENSP00000370989.3:n.-14-267_-14-266delinsTG
NM_001267706.1:c.-14-267_-14-266delinsTG	NP_001254635.1:n.-14-267_-14-266delinsTG
NM_001314029.1:c.-14-267_-14-266delinsTG	NP_001300958.1:n.-14-267_-14-266delinsTG
NM_014143.3:c.-14-267_-14-266delinsTG	NP_054862.1:n.-14-267_-14-266delinsTG
NR_052005.1:n.95-267_95-266delinsTG
XM_006716759.2:c.-14-267_-14-266delinsTG	XP_006716822.1:n.-14-267_-14-266delinsTG
NM_014143.4:c.-14-267_-14-266delinsTG MANE Select	NP_054862.1:n.-14-267_-14-266delinsTG
NM_001314029.2:c.-14-267_-14-266delinsTG	NP_001300958.1:n.-14-267_-14-266delinsTG
NR_052005.2:n.56-267_56-266delinsTG
NM_001267706.2:c.-14-267_-14-266delinsTG	NP_001254635.1:n.-14-267_-14-266delinsTG