Canonical Allele Identifier: CA2653107719
Gene: PCIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947891_45947894dup , CM000682.2:g.45947891_45947894dup GRCh38
NC_000020.10:g.44576530_44576533dup , CM000682.1:g.44576530_44576533dup GRCh37
NC_000020.9:g.44009937_44009940dup NCBI36
NG_029772.1:g.29302_29305dup

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*136_*139dup MANE Select ENSP00000361486.3:n.*136_*139dup
ENST00000372409.7:c.*136_*139dup ENSP00000361486.3:n.*136_*139dup
ENST00000479348.2:c.1192_1195dup
NM_022104.3:c.*136_*139dup NP_071387.1:n.*136_*139dup
XM_011528980.1:c.*136_*139dup XP_011527282.1:n.*136_*139dup
XM_011528981.1:c.*136_*139dup XP_011527283.1:n.*136_*139dup
XM_011528982.1:c.*136_*139dup XP_011527284.1:n.*136_*139dup
XM_011528980.3:c.*136_*139dup XP_011527282.1:n.*136_*139dup
XM_011528981.3:c.*136_*139dup XP_011527283.1:n.*136_*139dup
XM_017028013.2:c.*136_*139dup XP_016883502.1:n.*136_*139dup
XM_017028014.2:c.*136_*139dup XP_016883503.1:n.*136_*139dup
NM_022104.4:c.*136_*139dup MANE Select NP_071387.1:n.*136_*139dup