Canonical Allele Identifier: CA13092701
Gene: RCL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4834394A>G , CM000671.2:g.4834394A>G GRCh38
NC_000009.11:g.4834394A>G , CM000671.1:g.4834394A>G GRCh37
NC_000009.10:g.4824394A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381750.9:c.584+129A>G MANE Select ENSP00000371169.4:n.584+129A>G
ENST00000381750.8:c.584+129A>G ENSP00000371169.4:n.584+129A>G
ENST00000442869.5:c.110+129A>G ENSP00000412000.2:n.110+129A>G
ENST00000473230.1:n.288+1166A>G
NM_001286699.1:c.110+129A>G NP_001273628.1:n.110+129A>G
NM_001286700.1:c.110+129A>G NP_001273629.1:n.110+129A>G
NM_005772.4:c.584+129A>G NP_005763.3:n.584+129A>G
XM_006716715.2:c.260+129A>G XP_006716778.1:n.260+129A>G
XM_006716715.3:c.260+129A>G XP_006716778.1:n.260+129A>G
NM_005772.5:c.584+129A>G MANE Select NP_005763.3:n.584+129A>G
NM_001286699.2:c.110+129A>G NP_001273628.1:n.110+129A>G
NM_001286700.2:c.110+129A>G NP_001273629.1:n.110+129A>G