Canonical Allele Identifier: CA372837376

Gene: CD274

Linked Data

• dbSNP Id: rs17718883
• gnomAD v4: 9-5462876-C-A
• MyVariant Identifiers: chr9:g.5462876C>A (hg19) ; chr9:g.5462876C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000381577.4:c.437C>A MANE Select	ENSP00000370989.3:p.Pro146Gln
ENST00000381573.8:c.95C>A	ENSP00000370985.4:p.Pro32Gln
ENST00000381577.3:c.437C>A	ENSP00000370989.3:p.Pro146Gln
ENST00000474218.1:n.80C>A
ENST00000498261.1:n.437C>A
NM_001267706.1:c.95C>A	NP_001254635.1:p.Pro32Gln
NM_001314029.1:c.437C>A	NP_001300958.1:p.Pro146Gln
NM_014143.3:c.437C>A	NP_054862.1:p.Pro146Gln
NR_052005.1:n.545C>A
XM_006716759.2:c.437C>A	XP_006716822.1:p.Pro146Gln
NM_014143.4:c.437C>A MANE Select	NP_054862.1:p.Pro146Gln
NM_001314029.2:c.437C>A	NP_001300958.1:p.Pro146Gln
NR_052005.2:n.506C>A
NM_001267706.2:c.95C>A	NP_001254635.1:p.Pro32Gln