Canonical Allele Identifier: CA2366447929

Gene: PCIF1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45947777_45947778delinsGC , CM000682.2:g.45947777_45947778delinsGC	GRCh38
NC_000020.10:g.44576416_44576417delinsGC , CM000682.1:g.44576416_44576417delinsGC	GRCh37
NC_000020.9:g.44009823_44009824delinsGC	NCBI36
NG_029772.1:g.29417_29418delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000372409.8:c.*22_*23delinsGC MANE Select	ENSP00000361486.3:n.*22_*23delinsGC
ENST00000372409.7:c.*22_*23delinsGC	ENSP00000361486.3:n.*22_*23delinsGC
ENST00000479348.2:c.1078_1079delinsGC
NM_022104.3:c.*22_*23delinsGC	NP_071387.1:n.*22_*23delinsGC
XM_011528980.1:c.*22_*23delinsGC	XP_011527282.1:n.*22_*23delinsGC
XM_011528981.1:c.*22_*23delinsGC	XP_011527283.1:n.*22_*23delinsGC
XM_011528982.1:c.*22_*23delinsGC	XP_011527284.1:n.*22_*23delinsGC
XM_011528980.3:c.*22_*23delinsGC	XP_011527282.1:n.*22_*23delinsGC
XM_011528981.3:c.*22_*23delinsGC	XP_011527283.1:n.*22_*23delinsGC
XM_017028013.2:c.*22_*23delinsGC	XP_016883502.1:n.*22_*23delinsGC
XM_017028014.2:c.*22_*23delinsGC	XP_016883503.1:n.*22_*23delinsGC
NM_022104.4:c.*22_*23delinsGC MANE Select	NP_071387.1:n.*22_*23delinsGC