Canonical Allele Identifier: CA2653107636
Gene: PCIF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947775_45947777dup , CM000682.2:g.45947775_45947777dup GRCh38
NC_000020.10:g.44576414_44576416dup , CM000682.1:g.44576414_44576416dup GRCh37
NC_000020.9:g.44009821_44009823dup NCBI36
NG_029772.1:g.29425_29427dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.*20_*22dup MANE Select ENSP00000361486.3:n.*20_*22dup
ENST00000372409.7:c.*20_*22dup ENSP00000361486.3:n.*20_*22dup
ENST00000479348.2:c.1076_1078dup
NM_022104.3:c.*20_*22dup NP_071387.1:n.*20_*22dup
XM_011528980.1:c.*20_*22dup XP_011527282.1:n.*20_*22dup
XM_011528981.1:c.*20_*22dup XP_011527283.1:n.*20_*22dup
XM_011528982.1:c.*20_*22dup XP_011527284.1:n.*20_*22dup
XM_011528980.3:c.*20_*22dup XP_011527282.1:n.*20_*22dup
XM_011528981.3:c.*20_*22dup XP_011527283.1:n.*20_*22dup
XM_017028013.2:c.*20_*22dup XP_016883502.1:n.*20_*22dup
XM_017028014.2:c.*20_*22dup XP_016883503.1:n.*20_*22dup
NM_022104.4:c.*20_*22dup MANE Select NP_071387.1:n.*20_*22dup
Search 100 bp 5'
Search 100 bp 3'