Canonical Allele Identifier: CA1094122410

Gene: RNF217

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125009775G>T , CM000668.2:g.125009775G>T	GRCh38
NC_000006.11:g.125330921G>T , CM000668.1:g.125330921G>T	GRCh37
NC_000006.10:g.125372620G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521654.7:c.883-35436G>T MANE Select	ENSP00000428698.2:n.883-35436G>T
ENST00000359704.2:c.6+493G>T	ENSP00000352734.2:n.6+493G>T
ENST00000368414.6:c.-433+13120G>T	ENSP00000357399.2:n.-433+13120G>T
ENST00000454842.2:n.345-35436G>T
ENST00000519565.5:c.218-35436G>T
ENST00000521654.6:c.883-35436G>T	ENSP00000428698.2:n.883-35436G>T
ENST00000560949.5:c.100-35436G>T	ENSP00000452812.2:n.100-35436G>T
NM_001286398.1:c.883-35436G>T	NP_001273327.1:n.883-35436G>T
NM_152553.3:c.6+493G>T	NP_689766.1:n.6+493G>T
NR_104440.1:n.239+13120G>T
XM_011535494.1:c.883-35436G>T	XP_011533796.1:n.883-35436G>T
XM_011535496.1:c.882+46349G>T	XP_011533798.1:n.882+46349G>T
XM_011535497.1:c.883-35436G>T	XP_011533799.1:n.883-35436G>T
XM_011535498.1:c.1052-35436G>T	XP_011533800.1:n.1052-35436G>T
XM_011535500.1:c.25-35436G>T	XP_011533802.1:n.25-35436G>T
XR_942305.1:n.927-35436G>T
XR_942306.1:n.1698+493G>T
XR_942307.1:n.1409-239G>T
XR_942308.1:n.1299+13120G>T
XR_942310.1:n.1217-239G>T
NM_001286398.2:c.883-35436G>T	NP_001273327.1:n.883-35436G>T
NM_152553.4:c.6+493G>T	NP_689766.1:n.6+493G>T
NR_104440.2:n.239+13120G>T
NR_136734.1:n.1004-35436G>T
XM_011535494.2:c.883-35436G>T	XP_011533796.1:n.883-35436G>T
XM_011535496.2:c.882+46349G>T	XP_011533798.1:n.882+46349G>T
XM_011535500.2:c.25-35436G>T	XP_011533802.1:n.25-35436G>T
XR_001743178.1:n.1002-35436G>T
XR_001743179.1:n.1187-35436G>T
XR_001743181.1:n.1097+13120G>T
XR_942305.3:n.1002-35436G>T
NM_152553.5:c.6+493G>T	NP_689766.1:n.6+493G>T
NR_104440.3:n.235+13120G>T
NM_001286398.3:c.883-35436G>T MANE Select	NP_001273327.1:n.883-35436G>T