Canonical Allele Identifier: CA2366448021

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947925_45947926delinsTC , CM000682.2:g.45947925_45947926delinsTC	GRCh38
NC_000020.10:g.44576564_44576565delinsTC , CM000682.1:g.44576564_44576565delinsTC	GRCh37
NC_000020.9:g.44009971_44009972delinsTC	NCBI36
NG_029772.1:g.29269_29270delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372409.8:c.*170_*171delinsTC MANE Select	ENSP00000361486.3:n.*170_*171delinsTC
ENST00000372409.7:c.*170_*171delinsTC	ENSP00000361486.3:n.*170_*171delinsTC
ENST00000479348.2:c.1226_1227delinsTC
NM_022104.3:c.*170_*171delinsTC	NP_071387.1:n.*170_*171delinsTC
XM_011528980.1:c.*170_*171delinsTC	XP_011527282.1:n.*170_*171delinsTC
XM_011528981.1:c.*170_*171delinsTC	XP_011527283.1:n.*170_*171delinsTC
XM_011528982.1:c.*170_*171delinsTC	XP_011527284.1:n.*170_*171delinsTC
XM_011528980.3:c.*170_*171delinsTC	XP_011527282.1:n.*170_*171delinsTC
XM_011528981.3:c.*170_*171delinsTC	XP_011527283.1:n.*170_*171delinsTC
XM_017028013.2:c.*170_*171delinsTC	XP_016883502.1:n.*170_*171delinsTC
XM_017028014.2:c.*170_*171delinsTC	XP_016883503.1:n.*170_*171delinsTC
NM_022104.4:c.*170_*171delinsTC MANE Select	NP_071387.1:n.*170_*171delinsTC