Canonical Allele Identifier: CA1202094383
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886791_159886792delinsGT , CM000663.2:g.159886791_159886792delinsGT GRCh38
NC_000001.10:g.159856581_159856582delinsGT , CM000663.1:g.159856581_159856582delinsGT GRCh37
NC_000001.9:g.158123205_158123206delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-103_589-102delinsAC MANE Select ENSP00000357079.4:n.589-103_589-102delinsAC
ENST00000368099.8:c.589-103_589-102delinsAC ENSP00000357079.4:n.589-103_589-102delinsAC
ENST00000426543.6:c.334-103_334-102delinsAC ENSP00000403044.2:n.334-103_334-102delinsAC
ENST00000476696.5:c.589-103_589-102delinsAC ENSP00000483972.1:n.589-103_589-102delinsAC
ENST00000479940.2:c.334-103_334-102delinsAC ENSP00000478944.1:n.334-103_334-102delinsAC
NM_012337.2:c.589-103_589-102delinsAC NP_036469.2:n.589-103_589-102delinsAC
NM_012337.3:c.589-103_589-102delinsAC MANE Select NP_036469.2:n.589-103_589-102delinsAC