Canonical Allele Identifier: CA2366447688
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947335C= , CM000682.2:g.45947335C= GRCh38
NC_000020.10:g.44575974C= , CM000682.1:g.44575974C= GRCh37
NC_000020.9:g.44009381C= NCBI36
NG_029772.1:g.29860G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1780C= MANE Select ENSP00000361486.3:p.Pro594=
ENST00000372409.7:c.1780C= ENSP00000361486.3:p.Pro594=
ENST00000479348.2:c.636C=
NM_022104.3:c.1780C= NP_071387.1:p.Pro594=
XM_011528980.1:c.1780C= XP_011527282.1:p.Pro594=
XM_011528981.1:c.1780C= XP_011527283.1:p.Pro594=
XM_011528982.1:c.736C= XP_011527284.1:p.Pro246=
XM_011528980.3:c.1780C= XP_011527282.1:p.Pro594=
XM_011528981.3:c.1780C= XP_011527283.1:p.Pro594=
XM_017028013.2:c.1780C= XP_016883502.1:p.Pro594=
XM_017028014.2:c.736C= XP_016883503.1:p.Pro246=
NM_022104.4:c.1780C= MANE Select NP_071387.1:p.Pro594=