Canonical Allele Identifier: CA1217885131

Gene: CFHR5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995969_196995973delinsAACAG , CM000663.2:g.196995969_196995973delinsAACAG	GRCh38
NC_000001.10:g.196965099_196965103delinsAACAG , CM000663.1:g.196965099_196965103delinsAACAG	GRCh37
NC_000001.9:g.195231722_195231726delinsAACAG	NCBI36
NG_016365.1:g.23433_23437delinsAACAG , LRG_227:g.23433_23437delinsAACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.536-53_536-49delinsAACAG	ENSP00000514393.1:n.536-53_536-49delinsAACAG
ENST00000699467.1:n.860-53_860-49delinsAACAG
ENST00000699468.1:c.-24-145_-24-141delinsAACAG	ENSP00000514394.1:n.-24-145_-24-141delinsAACAG
ENST00000256785.5:c.791-53_791-49delinsAACAG MANE Select	ENSP00000256785.4:n.791-53_791-49delinsAACAG
ENST00000256785.4:c.791-53_791-49delinsAACAG	ENSP00000256785.4:n.791-53_791-49delinsAACAG
NM_030787.3:c.791-53_791-49delinsAACAG , LRG_227t1:c.791-53_791-49delinsAACAG	NP_110414.1:n.791-53_791-49delinsAACAG
XM_011510020.1:c.800-53_800-49delinsAACAG	XP_011508322.1:n.800-53_800-49delinsAACAG
XM_011510020.2:c.800-53_800-49delinsAACAG	XP_011508322.1:n.800-53_800-49delinsAACAG
NM_030787.4:c.791-53_791-49delinsAACAG MANE Select	NP_110414.1:n.791-53_791-49delinsAACAG