Canonical Allele Identifier: CA4815252

Gene: CFAP418 CFAP418-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.95269027C>T , CM000670.2:g.95269027C>T	GRCh38
NC_000008.10:g.96281255C>T , CM000670.1:g.96281255C>T	GRCh37
NC_000008.9:g.96350431C>T	NCBI36
NG_032804.1:g.5208G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_177965.4:c.155+8G>A (CFAP418) MANE Select	NP_808880.1:n.155+8G>A
ENST00000286688.6:c.155+8G>A (CFAP418) MANE Select	ENSP00000286688.5:n.155+8G>A
NM_001363260.1:c.155+8G>A (CFAP418)	NP_001350189.1:n.155+8G>A
NM_177965.3:c.155+8G>A (CFAP418)	NP_808880.1:n.155+8G>A
NR_038201.1:n.55+137C>T (CFAP418-AS1)
NR_038202.1:n.55+137C>T (CFAP418-AS1)
NR_038203.1:n.55+137C>T (CFAP418-AS1)
NR_038204.1:n.55+137C>T (CFAP418-AS1)
NR_038205.1:n.55+137C>T (CFAP418-AS1)
NR_038206.1:n.55+137C>T (CFAP418-AS1)
NR_038207.1:n.55+137C>T (CFAP418-AS1)
NR_038208.1:n.55+137C>T (CFAP418-AS1)
NR_038209.1:n.55+137C>T (CFAP418-AS1)
ENST00000286688.5:c.155+8G>A (CFAP418)	ENSP00000286688.5:n.155+8G>A
XM_005250799.2:c.494+8G>A (CFAP418)	XP_005250856.2:n.494+8G>A