Canonical Allele Identifier: CA1829549239

Gene: RCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4844265T= , CM000671.2:g.4844265T=	GRCh38
NC_000009.11:g.4844265T= , CM000671.1:g.4844265T=	GRCh37
NC_000009.10:g.4834265T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381750.9:c.711-260T= MANE Select	ENSP00000371169.4:n.711-260T=
ENST00000381728.5:c.153-260T=	ENSP00000371147.1:n.153-260T=
ENST00000381730.5:c.153-260T=	ENSP00000371149.1:n.153-260T=
ENST00000381750.8:c.711-260T=	ENSP00000371169.4:n.711-260T=
ENST00000441844.2:c.153-260T=	ENSP00000413381.1:n.153-260T=
ENST00000442869.5:c.237-260T=	ENSP00000412000.2:n.237-260T=
ENST00000448872.6:c.153-260T=	ENSP00000388096.2:n.153-260T=
NM_001286699.1:c.237-260T=	NP_001273628.1:n.237-260T=
NM_001286700.1:c.237-260T=	NP_001273629.1:n.237-260T=
NM_001286701.1:c.153-260T=	NP_001273630.1:n.153-260T=
NM_005772.4:c.711-260T=	NP_005763.3:n.711-260T=
XM_006716715.2:c.387-260T=	XP_006716778.1:n.387-260T=
XM_011517673.1:c.153-260T=	XP_011515975.1:n.153-260T=
XM_006716715.3:c.387-260T=	XP_006716778.1:n.387-260T=
XM_011517673.3:c.153-260T=	XP_011515975.1:n.153-260T=
XM_017014176.1:c.153-260T=	XP_016869665.1:n.153-260T=
NM_005772.5:c.711-260T= MANE Select	NP_005763.3:n.711-260T=
NM_001286699.2:c.237-260T=	NP_001273628.1:n.237-260T=
NM_001286700.2:c.237-260T=	NP_001273629.1:n.237-260T=
NM_001286701.2:c.153-260T=	NP_001273630.1:n.153-260T=