Canonical Allele Identifier: CA371838255
Gene: CFAP418 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.537T>G MANE Select ENSP00000286688.5:p.Tyr179Ter
ENST00000286688.5:c.537T>G ENSP00000286688.5:p.Tyr179Ter
NM_177965.3:c.537T>G NP_808880.1:p.Tyr179Ter
XM_005250799.2:c.780T>G XP_005250856.2:p.Tyr260Ter
NM_001363260.1:c.441T>G NP_001350189.1:p.Tyr147Ter
NM_177965.4:c.537T>G MANE Select NP_808880.1:p.Tyr179Ter