Canonical Allele Identifier: CA1829883049
Gene: CD274 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5468269A= , CM000671.2:g.5468269A= GRCh38
NC_000009.11:g.5468269A= , CM000671.1:g.5468269A= GRCh37
NC_000009.10:g.5458269A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.*407A= MANE Select ENSP00000370989.3:n.*407A=
ENST00000381573.8:c.*407A= ENSP00000370985.4:n.*407A=
ENST00000381577.3:c.*407A= ENSP00000370989.3:n.*407A=
NM_001267706.1:c.*407A= NP_001254635.1:n.*407A=
NM_014143.3:c.*407A= NP_054862.1:n.*407A=
NR_052005.1:n.1215A=
NM_014143.4:c.*407A= MANE Select NP_054862.1:n.*407A=
NR_052005.2:n.1176A=
NM_001267706.2:c.*407A= NP_001254635.1:n.*407A=
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