Canonical Allele Identifier: CA2687989273
Gene: CFAP418 HGNC NCBI

Linked Data

gnomAD v4: 8-95260448-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95260448C>G , CM000670.2:g.95260448C>G GRCh38
NC_000008.10:g.96272676C>G , CM000670.1:g.96272676C>G GRCh37
NC_000008.9:g.96341852C>G NCBI36
NG_032804.1:g.13787G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286688.6:c.308+20G>C MANE Select ENSP00000286688.5:n.308+20G>C
ENST00000286688.5:c.308+20G>C ENSP00000286688.5:n.308+20G>C
NM_177965.3:c.308+20G>C NP_808880.1:n.308+20G>C
XM_005250799.2:c.647+20G>C XP_005250856.2:n.647+20G>C
NM_001363260.1:c.308+20G>C NP_001350189.1:n.308+20G>C
NM_177965.4:c.308+20G>C MANE Select NP_808880.1:n.308+20G>C
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