Canonical Allele Identifier: CA1803877963

Gene: CFAP418

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.95260441T= , CM000670.2:g.95260441T=	GRCh38
NC_000008.10:g.96272669T= , CM000670.1:g.96272669T=	GRCh37
NC_000008.9:g.96341845T=	NCBI36
NG_032804.1:g.13794A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000286688.6:c.308+27A= MANE Select	ENSP00000286688.5:n.308+27A=
ENST00000286688.5:c.308+27A=	ENSP00000286688.5:n.308+27A=
NM_177965.3:c.308+27A=	NP_808880.1:n.308+27A=
XM_005250799.2:c.647+27A=	XP_005250856.2:n.647+27A=
NM_001363260.1:c.308+27A=	NP_001350189.1:n.308+27A=
NM_177965.4:c.308+27A= MANE Select	NP_808880.1:n.308+27A=