Canonical Allele Identifier: CA462360803
Gene: CFAP418 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.96259851T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247623T>C , CM000670.2:g.95247623T>C GRCh38
NC_000008.10:g.96259851T>C , CM000670.1:g.96259851T>C GRCh37
NC_000008.9:g.96329027T>C NCBI36
NG_032804.1:g.26612A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.618A>G MANE Select ENSP00000286688.5:p.Lys206=
ENST00000286688.5:c.618A>G ENSP00000286688.5:p.Lys206=
NM_177965.3:c.618A>G NP_808880.1:p.Lys206=
XM_005250799.2:c.861A>G XP_005250856.2:p.Lys287=
NM_001363260.1:c.522A>G NP_001350189.1:p.Lys174=
NM_177965.4:c.618A>G MANE Select NP_808880.1:p.Lys206=