Canonical Allele Identifier: CA422802677

Gene: CFHR5

Linked Data

• MyVariant Identifiers: chr1:g.196964890T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995760T>G , CM000663.2:g.196995760T>G	GRCh38
NC_000001.10:g.196964890T>G , CM000663.1:g.196964890T>G	GRCh37
NC_000001.9:g.195231513T>G	NCBI36
NG_016365.1:g.23224T>G , LRG_227:g.23224T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.396T>G	ENSP00000514393.1:p.Gly132=
ENST00000699467.1:n.720T>G
ENST00000699468.1:c.-24-354T>G	ENSP00000514394.1:n.-24-354T>G
ENST00000256785.5:c.651T>G MANE Select	ENSP00000256785.4:p.Gly217=
ENST00000256785.4:c.651T>G	ENSP00000256785.4:p.Gly217=
NM_030787.3:c.651T>G , LRG_227t1:c.651T>G	NP_110414.1:p.Gly217=
XM_011510020.1:c.660T>G	XP_011508322.1:p.Gly220=
XM_011510020.2:c.660T>G	XP_011508322.1:p.Gly220=
NM_030787.4:c.651T>G MANE Select	NP_110414.1:p.Gly217=