Canonical Allele Identifier: CA2617391446

Gene: C1R

Linked Data

• gnomAD v4: 12-7086491-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086491C>T , CM000674.2:g.7086491C>T	GRCh38
NG_062465.1:g.11117G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1039-34G>A MANE Select	ENSP00000497341.1:n.1039-34G>A
ENST00000648162.1:n.1011-34G>A
ENST00000649804.1:c.133-34G>A	ENSP00000497938.1:n.133-34G>A
ENST00000535233.6:c.937-34G>A	ENSP00000438636.3:n.937-34G>A
ENST00000536053.6:c.1081-34G>A	ENSP00000444271.3:n.1081-34G>A
ENST00000540394.5:n.2104-34G>A
ENST00000542285.5:c.1039-34G>A	ENSP00000438615.2:n.1039-34G>A
ENST00000602298.2:n.1354G>A
NM_001733.4:c.1039-34G>A	NP_001724.3:n.1039-34G>A
NM_001354346.1:c.1081-34G>A	NP_001341275.1:n.1081-34G>A
NM_001733.6:c.1039-34G>A	NP_001724.4:n.1039-34G>A
NM_001733.7:c.1039-34G>A MANE Select	NP_001724.4:n.1039-34G>A
NM_001354346.2:c.1081-34G>A	NP_001341275.1:n.1081-34G>A