Canonical Allele Identifier: CA1829879666
Community Standard Title: NM_014143.4(CD274):c.683-369C=
Gene: CD274 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5465130C= , CM000671.2:g.5465130C= GRCh38
NC_000009.11:g.5465130C= , CM000671.1:g.5465130C= GRCh37
NC_000009.10:g.5455130C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014143.4:c.683-369C= MANE Select NP_054862.1:n.683-369C=
ENST00000381577.4:c.683-369C= MANE Select ENSP00000370989.3:n.683-369C=
NM_001267706.1:c.341-369C= NP_001254635.1:n.341-369C=
NM_001267706.2:c.341-369C= NP_001254635.1:n.341-369C=
NM_014143.3:c.683-369C= NP_054862.1:n.683-369C=
NR_052005.1:n.685-369C=
NR_052005.2:n.646-369C=
ENST00000381573.8:c.341-369C= ENSP00000370985.4:n.341-369C=
ENST00000381577.3:c.683-369C= ENSP00000370989.3:n.683-369C=
ENST00000492923.1:n.188-369C=
ENST00000498261.1:n.577-369C=
XM_006716759.2:c.*40-369C= XP_006716822.1:n.*40-369C=