Canonical Allele Identifier: CA2648611206

Gene: CFAP45

Linked Data

• gnomAD v4: 1-159886776-G-GTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886776_159886777insTAT , CM000663.2:g.159886776_159886777insTAT	GRCh38
NC_000001.10:g.159856566_159856567insTAT , CM000663.1:g.159856566_159856567insTAT	GRCh37
NC_000001.9:g.158123190_158123191insTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.589-88_589-87insATA MANE Select	ENSP00000357079.4:n.589-88_589-87insATA
ENST00000368099.8:c.589-88_589-87insATA	ENSP00000357079.4:n.589-88_589-87insATA
ENST00000426543.6:c.334-88_334-87insATA	ENSP00000403044.2:n.334-88_334-87insATA
ENST00000476696.5:c.589-88_589-87insATA	ENSP00000483972.1:n.589-88_589-87insATA
ENST00000479940.2:c.334-88_334-87insATA	ENSP00000478944.1:n.334-88_334-87insATA
NM_012337.2:c.589-88_589-87insATA	NP_036469.2:n.589-88_589-87insATA
NM_012337.3:c.589-88_589-87insATA MANE Select	NP_036469.2:n.589-88_589-87insATA