Canonical Allele Identifier: CA2816513977
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947923A>G , CM000682.2:g.45947923A>G GRCh38
NC_000020.10:g.44576562A>G , CM000682.1:g.44576562A>G GRCh37
NC_000020.9:g.44009969A>G NCBI36
NG_029772.1:g.29272T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.*168A>G MANE Select ENSP00000361486.3:n.*168A>G
ENST00000372409.7:c.*168A>G ENSP00000361486.3:n.*168A>G
ENST00000479348.2:c.1224A>G
NM_022104.3:c.*168A>G NP_071387.1:n.*168A>G
XM_011528980.1:c.*168A>G XP_011527282.1:n.*168A>G
XM_011528981.1:c.*168A>G XP_011527283.1:n.*168A>G
XM_011528982.1:c.*168A>G XP_011527284.1:n.*168A>G
XM_011528980.3:c.*168A>G XP_011527282.1:n.*168A>G
XM_011528981.3:c.*168A>G XP_011527283.1:n.*168A>G
XM_017028013.2:c.*168A>G XP_016883502.1:n.*168A>G
XM_017028014.2:c.*168A>G XP_016883503.1:n.*168A>G
NM_022104.4:c.*168A>G MANE Select NP_071387.1:n.*168A>G