Canonical Allele Identifier: CA2366447936

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947781_45947782delinsCA , CM000682.2:g.45947781_45947782delinsCA	GRCh38
NC_000020.10:g.44576420_44576421delinsCA , CM000682.1:g.44576420_44576421delinsCA	GRCh37
NC_000020.9:g.44009827_44009828delinsCA	NCBI36
NG_029772.1:g.29413_29414delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000372409.8:c.*26_*27delinsCA MANE Select	ENSP00000361486.3:n.*26_*27delinsCA
ENST00000372409.7:c.*26_*27delinsCA	ENSP00000361486.3:n.*26_*27delinsCA
ENST00000479348.2:c.1082_1083delinsCA
NM_022104.3:c.*26_*27delinsCA	NP_071387.1:n.*26_*27delinsCA
XM_011528980.1:c.*26_*27delinsCA	XP_011527282.1:n.*26_*27delinsCA
XM_011528981.1:c.*26_*27delinsCA	XP_011527283.1:n.*26_*27delinsCA
XM_011528982.1:c.*26_*27delinsCA	XP_011527284.1:n.*26_*27delinsCA
XM_011528980.3:c.*26_*27delinsCA	XP_011527282.1:n.*26_*27delinsCA
XM_011528981.3:c.*26_*27delinsCA	XP_011527283.1:n.*26_*27delinsCA
XM_017028013.2:c.*26_*27delinsCA	XP_016883502.1:n.*26_*27delinsCA
XM_017028014.2:c.*26_*27delinsCA	XP_016883503.1:n.*26_*27delinsCA
NM_022104.4:c.*26_*27delinsCA MANE Select	NP_071387.1:n.*26_*27delinsCA