Canonical Allele Identifier: CA2366447690
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947337A= , CM000682.2:g.45947337A= GRCh38
NC_000020.10:g.44575976A= , CM000682.1:g.44575976A= GRCh37
NC_000020.9:g.44009383A= NCBI36
NG_029772.1:g.29858T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1782A= MANE Select ENSP00000361486.3:p.Pro594=
ENST00000372409.7:c.1782A= ENSP00000361486.3:p.Pro594=
ENST00000479348.2:c.638A=
NM_022104.3:c.1782A= NP_071387.1:p.Pro594=
XM_011528980.1:c.1782A= XP_011527282.1:p.Pro594=
XM_011528981.1:c.1782A= XP_011527283.1:p.Pro594=
XM_011528982.1:c.738A= XP_011527284.1:p.Pro246=
XM_011528980.3:c.1782A= XP_011527282.1:p.Pro594=
XM_011528981.3:c.1782A= XP_011527283.1:p.Pro594=
XM_017028013.2:c.1782A= XP_016883502.1:p.Pro594=
XM_017028014.2:c.738A= XP_016883503.1:p.Pro246=
NM_022104.4:c.1782A= MANE Select NP_071387.1:p.Pro594=