Canonical Allele Identifier: CA2838220189
Gene: RPAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41536267dup , CM000677.2:g.41536267dup GRCh38
NC_000015.9:g.41828465dup , CM000677.1:g.41828465dup GRCh37
NC_000015.8:g.39615757dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000304330.9:c.331-46dup MANE Select ENSP00000306123.4:n.331-46dup
ENST00000304330.8:c.331-46dup ENSP00000306123.4:n.331-46dup
ENST00000561603.5:c.331-46dup ENSP00000456207.1:n.331-46dup
ENST00000562303.5:c.331-46dup ENSP00000455363.1:n.331-46dup
ENST00000563293.1:n.112dup
ENST00000566863.1:c.331-46dup ENSP00000455527.1:n.331-46dup
ENST00000567866.5:c.331-46dup ENSP00000455381.1:n.331-46dup
NM_015540.3:c.331-46dup NP_056355.2:n.331-46dup
XM_005254297.1:c.331-46dup XP_005254354.1:n.331-46dup
XM_006720469.1:c.331-46dup XP_006720532.1:n.331-46dup
NM_015540.4:c.331-46dup MANE Select NP_056355.2:n.331-46dup