Canonical Allele Identifier: CA2366447938

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947782_45947783delinsAG , CM000682.2:g.45947782_45947783delinsAG	GRCh38
NC_000020.10:g.44576421_44576422delinsAG , CM000682.1:g.44576421_44576422delinsAG	GRCh37
NC_000020.9:g.44009828_44009829delinsAG	NCBI36
NG_029772.1:g.29412_29413delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000372409.8:c.*27_*28delinsAG MANE Select	ENSP00000361486.3:n.*27_*28delinsAG
ENST00000372409.7:c.*27_*28delinsAG	ENSP00000361486.3:n.*27_*28delinsAG
ENST00000479348.2:c.1083_1084delinsAG
NM_022104.3:c.*27_*28delinsAG	NP_071387.1:n.*27_*28delinsAG
XM_011528980.1:c.*27_*28delinsAG	XP_011527282.1:n.*27_*28delinsAG
XM_011528981.1:c.*27_*28delinsAG	XP_011527283.1:n.*27_*28delinsAG
XM_011528982.1:c.*27_*28delinsAG	XP_011527284.1:n.*27_*28delinsAG
XM_011528980.3:c.*27_*28delinsAG	XP_011527282.1:n.*27_*28delinsAG
XM_011528981.3:c.*27_*28delinsAG	XP_011527283.1:n.*27_*28delinsAG
XM_017028013.2:c.*27_*28delinsAG	XP_016883502.1:n.*27_*28delinsAG
XM_017028014.2:c.*27_*28delinsAG	XP_016883503.1:n.*27_*28delinsAG
NM_022104.4:c.*27_*28delinsAG MANE Select	NP_071387.1:n.*27_*28delinsAG