Canonical Allele Identifier: CA1829535918

Gene: RCL1

Linked Data

• dbSNP Id: rs10758658

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4856877G>C , CM000671.2:g.4856877G>C	GRCh38
NC_000009.11:g.4856877G>C , CM000671.1:g.4856877G>C	GRCh37
NC_000009.10:g.4846877G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381750.9:c.972-3248G>C MANE Select	ENSP00000371169.4:n.972-3248G>C
ENST00000381728.5:c.414-3248G>C	ENSP00000371147.1:n.414-3248G>C
ENST00000381730.5:c.414-3248G>C	ENSP00000371149.1:n.414-3248G>C
ENST00000381750.8:c.972-3248G>C	ENSP00000371169.4:n.972-3248G>C
ENST00000442869.5:c.498-3248G>C	ENSP00000412000.2:n.498-3248G>C
ENST00000448872.6:c.414-3248G>C	ENSP00000388096.2:n.414-3248G>C
NM_001286699.1:c.498-3248G>C	NP_001273628.1:n.498-3248G>C
NM_001286700.1:c.498-3248G>C	NP_001273629.1:n.498-3248G>C
NM_001286701.1:c.414-3248G>C	NP_001273630.1:n.414-3248G>C
NM_005772.4:c.972-3248G>C	NP_005763.3:n.972-3248G>C
XM_006716715.2:c.648-3248G>C	XP_006716778.1:n.648-3248G>C
XM_011517673.1:c.414-3248G>C	XP_011515975.1:n.414-3248G>C
XM_006716715.3:c.648-3248G>C	XP_006716778.1:n.648-3248G>C
XM_011517673.3:c.414-3248G>C	XP_011515975.1:n.414-3248G>C
XM_017014176.1:c.414-3248G>C	XP_016869665.1:n.414-3248G>C
NM_005772.5:c.972-3248G>C MANE Select	NP_005763.3:n.972-3248G>C
NM_001286699.2:c.498-3248G>C	NP_001273628.1:n.498-3248G>C
NM_001286700.2:c.498-3248G>C	NP_001273629.1:n.498-3248G>C
NM_001286701.2:c.414-3248G>C	NP_001273630.1:n.414-3248G>C