Canonical Allele Identifier: CA422802665

Gene: CFHR5

Linked Data

• MyVariant Identifiers: chr1:g.196964881C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995751C>G , CM000663.2:g.196995751C>G	GRCh38
NC_000001.10:g.196964881C>G , CM000663.1:g.196964881C>G	GRCh37
NC_000001.9:g.195231504C>G	NCBI36
NG_016365.1:g.23215C>G , LRG_227:g.23215C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.387C>G	ENSP00000514393.1:p.Leu129=
ENST00000699467.1:n.711C>G
ENST00000699468.1:c.-24-363C>G	ENSP00000514394.1:n.-24-363C>G
ENST00000256785.5:c.642C>G MANE Select	ENSP00000256785.4:p.Leu214=
ENST00000256785.4:c.642C>G	ENSP00000256785.4:p.Leu214=
NM_030787.3:c.642C>G , LRG_227t1:c.642C>G	NP_110414.1:p.Leu214=
XM_011510020.1:c.651C>G	XP_011508322.1:p.Leu217=
XM_011510020.2:c.651C>G	XP_011508322.1:p.Leu217=
NM_030787.4:c.642C>G MANE Select	NP_110414.1:p.Leu214=