Canonical Allele Identifier: CA2653107670
Gene: PCIF1 HGNC NCBI

Linked Data

gnomAD v4: 20-45947816-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947816C>A , CM000682.2:g.45947816C>A GRCh38
NC_000020.10:g.44576455C>A , CM000682.1:g.44576455C>A GRCh37
NC_000020.9:g.44009862C>A NCBI36
NG_029772.1:g.29379G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*61C>A MANE Select ENSP00000361486.3:n.*61C>A
ENST00000372409.7:c.*61C>A ENSP00000361486.3:n.*61C>A
ENST00000479348.2:c.1117C>A
NM_022104.3:c.*61C>A NP_071387.1:n.*61C>A
XM_011528980.1:c.*61C>A XP_011527282.1:n.*61C>A
XM_011528981.1:c.*61C>A XP_011527283.1:n.*61C>A
XM_011528982.1:c.*61C>A XP_011527284.1:n.*61C>A
XM_011528980.3:c.*61C>A XP_011527282.1:n.*61C>A
XM_011528981.3:c.*61C>A XP_011527283.1:n.*61C>A
XM_017028013.2:c.*61C>A XP_016883502.1:n.*61C>A
XM_017028014.2:c.*61C>A XP_016883503.1:n.*61C>A
NM_022104.4:c.*61C>A MANE Select NP_071387.1:n.*61C>A
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