Canonical Allele Identifier: CA1829535866
Gene: RCL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4856836C= , CM000671.2:g.4856836C= GRCh38
NC_000009.11:g.4856836C= , CM000671.1:g.4856836C= GRCh37
NC_000009.10:g.4846836C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381750.9:c.972-3289C= MANE Select ENSP00000371169.4:n.972-3289C=
ENST00000381728.5:c.414-3289C= ENSP00000371147.1:n.414-3289C=
ENST00000381730.5:c.414-3289C= ENSP00000371149.1:n.414-3289C=
ENST00000381750.8:c.972-3289C= ENSP00000371169.4:n.972-3289C=
ENST00000442869.5:c.498-3289C= ENSP00000412000.2:n.498-3289C=
ENST00000448872.6:c.414-3289C= ENSP00000388096.2:n.414-3289C=
NM_001286699.1:c.498-3289C= NP_001273628.1:n.498-3289C=
NM_001286700.1:c.498-3289C= NP_001273629.1:n.498-3289C=
NM_001286701.1:c.414-3289C= NP_001273630.1:n.414-3289C=
NM_005772.4:c.972-3289C= NP_005763.3:n.972-3289C=
XM_006716715.2:c.648-3289C= XP_006716778.1:n.648-3289C=
XM_011517673.1:c.414-3289C= XP_011515975.1:n.414-3289C=
XM_006716715.3:c.648-3289C= XP_006716778.1:n.648-3289C=
XM_011517673.3:c.414-3289C= XP_011515975.1:n.414-3289C=
XM_017014176.1:c.414-3289C= XP_016869665.1:n.414-3289C=
NM_005772.5:c.972-3289C= MANE Select NP_005763.3:n.972-3289C=
NM_001286699.2:c.498-3289C= NP_001273628.1:n.498-3289C=
NM_001286700.2:c.498-3289C= NP_001273629.1:n.498-3289C=
NM_001286701.2:c.414-3289C= NP_001273630.1:n.414-3289C=