Canonical Allele Identifier: CA2366447979

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947850_45947852delinsCAT , CM000682.2:g.45947850_45947852delinsCAT	GRCh38
NC_000020.10:g.44576489_44576491delinsCAT , CM000682.1:g.44576489_44576491delinsCAT	GRCh37
NC_000020.9:g.44009896_44009898delinsCAT	NCBI36
NG_029772.1:g.29343_29345delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.*95_*97delinsCAT MANE Select	ENSP00000361486.3:n.*95_*97delinsCAT
ENST00000372409.7:c.*95_*97delinsCAT	ENSP00000361486.3:n.*95_*97delinsCAT
ENST00000479348.2:c.1151_1153delinsCAT
NM_022104.3:c.*95_*97delinsCAT	NP_071387.1:n.*95_*97delinsCAT
XM_011528980.1:c.*95_*97delinsCAT	XP_011527282.1:n.*95_*97delinsCAT
XM_011528981.1:c.*95_*97delinsCAT	XP_011527283.1:n.*95_*97delinsCAT
XM_011528982.1:c.*95_*97delinsCAT	XP_011527284.1:n.*95_*97delinsCAT
XM_011528980.3:c.*95_*97delinsCAT	XP_011527282.1:n.*95_*97delinsCAT
XM_011528981.3:c.*95_*97delinsCAT	XP_011527283.1:n.*95_*97delinsCAT
XM_017028013.2:c.*95_*97delinsCAT	XP_016883502.1:n.*95_*97delinsCAT
XM_017028014.2:c.*95_*97delinsCAT	XP_016883503.1:n.*95_*97delinsCAT
NM_022104.4:c.*95_*97delinsCAT MANE Select	NP_071387.1:n.*95_*97delinsCAT