Canonical Allele Identifier: CA478523080

Gene: C1R C1RL

Linked Data

• MyVariant Identifiers: chr12:g.7244219G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7091623G>C , CM000674.2:g.7091623G>C	GRCh38
NC_000012.11:g.7244219G>C , CM000674.1:g.7244219G>C	GRCh37
NC_000012.10:g.7135360G>C	NCBI36
NG_062465.1:g.5985C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.60C>G (C1R) MANE Select	ENSP00000497341.1:p.Pro20=
ENST00000535233.6:c.60C>G (C1R)	ENSP00000438636.3:p.Pro20=
ENST00000536053.6:c.102C>G (C1R)	ENSP00000444271.3:p.Pro34=
ENST00000536092.1:n.165C>G (C1R)
ENST00000538050.5:c.-256C>G (C1R)	ENSP00000444009.1:n.-256C>G
ENST00000539803.5:c.527C>G (C1RL)
ENST00000540242.2:c.60C>G (C1R)	ENSP00000442946.1:p.Pro20=
ENST00000540394.5:n.819C>G (C1R)
ENST00000540610.5:c.-85+764C>G (C1R)	ENSP00000439223.1:n.-85+764C>G
ENST00000541042.5:c.-256C>G (C1R)	ENSP00000441601.1:n.-256C>G
ENST00000542285.5:c.60C>G (C1R)	ENSP00000438615.2:p.Pro20=
ENST00000543362.5:c.60C>G (C1R)	ENSP00000446356.1:p.Pro20=
ENST00000543835.5:c.60C>G (C1R)	ENSP00000445285.1:p.Pro20=
ENST00000545466.1:n.113C>G (C1R)
NM_001733.4:c.60C>G (C1R)	NP_001724.3:p.Pro20=
NM_001354346.1:c.102C>G (C1R)	NP_001341275.1:p.Pro34=
NM_001733.6:c.60C>G (C1R)	NP_001724.4:p.Pro20=
NM_001733.7:c.60C>G (C1R) MANE Select	NP_001724.4:p.Pro20=
NM_001354346.2:c.102C>G (C1R)	NP_001341275.1:p.Pro34=