Canonical Allele Identifier: CA2617393826

Gene: C1R C1RL

Linked Data

• gnomAD v4: 12-7091448-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7091448C>A , CM000674.2:g.7091448C>A	GRCh38
NC_000012.11:g.7244044C>A , CM000674.1:g.7244044C>A	GRCh37
NC_000012.10:g.7135185C>A	NCBI36
NG_062465.1:g.6160G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.231+4G>T (C1R) MANE Select	ENSP00000497341.1:n.231+4G>T
ENST00000535233.6:c.231+4G>T (C1R)	ENSP00000438636.3:n.231+4G>T
ENST00000536053.6:c.273+4G>T (C1R)	ENSP00000444271.3:n.273+4G>T
ENST00000536092.1:n.340G>T (C1R)
ENST00000538050.5:c.-85+4G>T (C1R)	ENSP00000444009.1:n.-85+4G>T
ENST00000539803.5:c.698+4G>T (C1RL)
ENST00000540242.2:c.231+4G>T (C1R)	ENSP00000442946.1:n.231+4G>T
ENST00000540394.5:n.990+4G>T (C1R)
ENST00000540610.5:c.-85+939G>T (C1R)	ENSP00000439223.1:n.-85+939G>T
ENST00000541042.5:c.-85+4G>T (C1R)	ENSP00000441601.1:n.-85+4G>T
ENST00000542285.5:c.231+4G>T (C1R)	ENSP00000438615.2:n.231+4G>T
ENST00000543362.5:c.231+4G>T (C1R)	ENSP00000446356.1:n.231+4G>T
ENST00000543835.5:c.231+4G>T (C1R)	ENSP00000445285.1:n.231+4G>T
ENST00000545466.1:n.284+4G>T (C1R)
NM_001733.4:c.231+4G>T (C1R)	NP_001724.3:n.231+4G>T
NM_001354346.1:c.273+4G>T (C1R)	NP_001341275.1:n.273+4G>T
NM_001733.6:c.231+4G>T (C1R)	NP_001724.4:n.231+4G>T
NM_001733.7:c.231+4G>T (C1R) MANE Select	NP_001724.4:n.231+4G>T
NM_001354346.2:c.273+4G>T (C1R)	NP_001341275.1:n.273+4G>T