Canonical Allele Identifier: CA2366447857

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947669_45947671delinsGGT , CM000682.2:g.45947669_45947671delinsGGT	GRCh38
NC_000020.10:g.44576308_44576310delinsGGT , CM000682.1:g.44576308_44576310delinsGGT	GRCh37
NC_000020.9:g.44009715_44009717delinsGGT	NCBI36
NG_029772.1:g.29524_29526delinsACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000372409.8:c.2029_2031delinsGGT MANE Select	ENSP00000361486.3:p.Gly677=
ENST00000372409.7:c.2029_2031delinsGGT	ENSP00000361486.3:p.Gly677=
ENST00000479348.2:c.970_972delinsGGT
NM_022104.3:c.2029_2031delinsGGT	NP_071387.1:p.Gly677=
XM_011528980.1:c.2029_2031delinsGGT	XP_011527282.1:p.Gly677=
XM_011528981.1:c.2029_2031delinsGGT	XP_011527283.1:p.Gly677=
XM_011528982.1:c.985_987delinsGGT	XP_011527284.1:p.Gly329=
XM_011528980.3:c.2029_2031delinsGGT	XP_011527282.1:p.Gly677=
XM_011528981.3:c.2029_2031delinsGGT	XP_011527283.1:p.Gly677=
XM_017028013.2:c.2029_2031delinsGGT	XP_016883502.1:p.Gly677=
XM_017028014.2:c.985_987delinsGGT	XP_016883503.1:p.Gly329=
NM_022104.4:c.2029_2031delinsGGT MANE Select	NP_071387.1:p.Gly677=