Canonical Allele Identifier: CA2366448055

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947970_45947972delinsCCT , CM000682.2:g.45947970_45947972delinsCCT	GRCh38
NC_000020.10:g.44576609_44576611delinsCCT , CM000682.1:g.44576609_44576611delinsCCT	GRCh37
NC_000020.9:g.44010016_44010018delinsCCT	NCBI36
NG_029772.1:g.29223_29225delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.*215_*217delinsCCT MANE Select	ENSP00000361486.3:n.*215_*217delinsCCT
ENST00000372409.7:c.*215_*217delinsCCT	ENSP00000361486.3:n.*215_*217delinsCCT
ENST00000479348.2:c.1271_1273delinsCCT
NM_022104.3:c.*215_*217delinsCCT	NP_071387.1:n.*215_*217delinsCCT
XM_011528980.1:c.*215_*217delinsCCT	XP_011527282.1:n.*215_*217delinsCCT
XM_011528981.1:c.*215_*217delinsCCT	XP_011527283.1:n.*215_*217delinsCCT
XM_011528982.1:c.*215_*217delinsCCT	XP_011527284.1:n.*215_*217delinsCCT
XM_011528980.3:c.*215_*217delinsCCT	XP_011527282.1:n.*215_*217delinsCCT
XM_011528981.3:c.*215_*217delinsCCT	XP_011527283.1:n.*215_*217delinsCCT
XM_017028013.2:c.*215_*217delinsCCT	XP_016883502.1:n.*215_*217delinsCCT
XM_017028014.2:c.*215_*217delinsCCT	XP_016883503.1:n.*215_*217delinsCCT
NM_022104.4:c.*215_*217delinsCCT MANE Select	NP_071387.1:n.*215_*217delinsCCT