Canonical Allele Identifier: CA2366448073
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45948011_45948014delinsACCC , CM000682.2:g.45948011_45948014delinsACCC GRCh38
NC_000020.10:g.44576650_44576653delinsACCC , CM000682.1:g.44576650_44576653delinsACCC GRCh37
NC_000020.9:g.44010057_44010060delinsACCC NCBI36
NG_029772.1:g.29181_29184delinsGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.*256_*259delinsACCC MANE Select ENSP00000361486.3:n.*256_*259delinsACCC
ENST00000372409.7:c.*256_*259delinsACCC ENSP00000361486.3:n.*256_*259delinsACCC
ENST00000479348.2:c.1312_1315delinsACCC
NM_022104.3:c.*256_*259delinsACCC NP_071387.1:n.*256_*259delinsACCC
XM_011528980.1:c.*256_*259delinsACCC XP_011527282.1:n.*256_*259delinsACCC
XM_011528981.1:c.*256_*259delinsACCC XP_011527283.1:n.*256_*259delinsACCC
XM_011528982.1:c.*256_*259delinsACCC XP_011527284.1:n.*256_*259delinsACCC
XM_011528980.3:c.*256_*259delinsACCC XP_011527282.1:n.*256_*259delinsACCC
XM_011528981.3:c.*256_*259delinsACCC XP_011527283.1:n.*256_*259delinsACCC
XM_017028013.2:c.*256_*259delinsACCC XP_016883502.1:n.*256_*259delinsACCC
XM_017028014.2:c.*256_*259delinsACCC XP_016883503.1:n.*256_*259delinsACCC
NM_022104.4:c.*256_*259delinsACCC MANE Select NP_071387.1:n.*256_*259delinsACCC