Canonical Allele Identifier: CA1803867853

Gene: CFAP418

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.95247608T= , CM000670.2:g.95247608T=	GRCh38
NC_000008.10:g.96259836T= , CM000670.1:g.96259836T=	GRCh37
NC_000008.9:g.96329012T=	NCBI36
NG_032804.1:g.26627A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286688.6:c.*9A= MANE Select	ENSP00000286688.5:n.*9A=
ENST00000286688.5:c.*9A=	ENSP00000286688.5:n.*9A=
NM_177965.3:c.*9A=	NP_808880.1:n.*9A=
XM_005250799.2:c.*9A=	XP_005250856.2:n.*9A=
NM_001363260.1:c.*9A=	NP_001350189.1:n.*9A=
NM_177965.4:c.*9A= MANE Select	NP_808880.1:n.*9A=