Canonical Allele Identifier: CA2974733718

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947764_45947765insGGG , CM000682.2:g.45947764_45947765insGGG	GRCh38
NC_000020.10:g.44576403_44576404insGGG , CM000682.1:g.44576403_44576404insGGG	GRCh37
NC_000020.9:g.44009810_44009811insGGG	NCBI36
NG_029772.1:g.29431_29432insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.*9_*10insGGG MANE Select	ENSP00000361486.3:n.*9_*10insGGG
ENST00000372409.7:c.*9_*10insGGG	ENSP00000361486.3:n.*9_*10insGGG
ENST00000479348.2:c.1065_1066insGGG
NM_022104.3:c.*9_*10insGGG	NP_071387.1:n.*9_*10insGGG
XM_011528980.1:c.*9_*10insGGG	XP_011527282.1:n.*9_*10insGGG
XM_011528981.1:c.*9_*10insGGG	XP_011527283.1:n.*9_*10insGGG
XM_011528982.1:c.*9_*10insGGG	XP_011527284.1:n.*9_*10insGGG
XM_011528980.3:c.*9_*10insGGG	XP_011527282.1:n.*9_*10insGGG
XM_011528981.3:c.*9_*10insGGG	XP_011527283.1:n.*9_*10insGGG
XM_017028013.2:c.*9_*10insGGG	XP_016883502.1:n.*9_*10insGGG
XM_017028014.2:c.*9_*10insGGG	XP_016883503.1:n.*9_*10insGGG
NM_022104.4:c.*9_*10insGGG MANE Select	NP_071387.1:n.*9_*10insGGG