Canonical Allele Identifier: CA2366447926
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947776A= , CM000682.2:g.45947776A= GRCh38
NC_000020.10:g.44576415A= , CM000682.1:g.44576415A= GRCh37
NC_000020.9:g.44009822A= NCBI36
NG_029772.1:g.29419T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*21A= MANE Select ENSP00000361486.3:n.*21A=
ENST00000372409.7:c.*21A= ENSP00000361486.3:n.*21A=
ENST00000479348.2:c.1077A=
NM_022104.3:c.*21A= NP_071387.1:n.*21A=
XM_011528980.1:c.*21A= XP_011527282.1:n.*21A=
XM_011528981.1:c.*21A= XP_011527283.1:n.*21A=
XM_011528982.1:c.*21A= XP_011527284.1:n.*21A=
XM_011528980.3:c.*21A= XP_011527282.1:n.*21A=
XM_011528981.3:c.*21A= XP_011527283.1:n.*21A=
XM_017028013.2:c.*21A= XP_016883502.1:n.*21A=
XM_017028014.2:c.*21A= XP_016883503.1:n.*21A=
NM_022104.4:c.*21A= MANE Select NP_071387.1:n.*21A=