Canonical Allele Identifier: CA1829877320

Gene: CD274

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5462876C= , CM000671.2:g.5462876C=	GRCh38
NC_000009.11:g.5462876C= , CM000671.1:g.5462876C=	GRCh37
NC_000009.10:g.5452876C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014143.4:c.437C= MANE Select	NP_054862.1:p.Pro146=
ENST00000381577.4:c.437C= MANE Select	ENSP00000370989.3:p.Pro146=
NM_001267706.1:c.95C=	NP_001254635.1:p.Pro32=
NM_001267706.2:c.95C=	NP_001254635.1:p.Pro32=
NM_001314029.1:c.437C=	NP_001300958.1:p.Pro146=
NM_001314029.2:c.437C=	NP_001300958.1:p.Pro146=
NM_014143.3:c.437C=	NP_054862.1:p.Pro146=
NR_052005.1:n.545C=
NR_052005.2:n.506C=
ENST00000381573.8:c.95C=	ENSP00000370985.4:p.Pro32=
ENST00000381577.3:c.437C=	ENSP00000370989.3:p.Pro146=
ENST00000474218.1:n.80C=
ENST00000498261.1:n.437C=
XM_006716759.2:c.437C=	XP_006716822.1:p.Pro146=