Canonical Allele Identifier: CA1803868020
Gene: CFAP418 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247704A= , CM000670.2:g.95247704A= GRCh38
NC_000008.10:g.96259932A= , CM000670.1:g.96259932A= GRCh37
NC_000008.9:g.96329108A= NCBI36
NG_032804.1:g.26531T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.537T= MANE Select ENSP00000286688.5:p.Tyr179=
ENST00000286688.5:c.537T= ENSP00000286688.5:p.Tyr179=
NM_177965.3:c.537T= NP_808880.1:p.Tyr179=
XM_005250799.2:c.780T= XP_005250856.2:p.Tyr260=
NM_001363260.1:c.441T= NP_001350189.1:p.Tyr147=
NM_177965.4:c.537T= MANE Select NP_808880.1:p.Tyr179=