Canonical Allele Identifier: CA13714560

Gene: RNFT2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116761609G>T , CM000674.2:g.116761609G>T	GRCh38
NC_000012.11:g.117199414G>T , CM000674.1:g.117199414G>T	GRCh37
NC_000012.10:g.115683797G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257575.9:c.628-5205G>T MANE Select	ENSP00000257575.4:n.628-5205G>T
ENST00000392549.7:c.628-5205G>T	ENSP00000376332.2:n.628-5205G>T
ENST00000677328.1:c.-130+988G>T	ENSP00000504767.1:n.-130+988G>T
ENST00000257575.8:c.628-5205G>T	ENSP00000257575.4:n.628-5205G>T
ENST00000319176.11:c.628-5205G>T	ENSP00000321405.8:n.628-5205G>T
ENST00000392549.6:c.628-5205G>T	ENSP00000376332.2:n.628-5205G>T
ENST00000407967.7:c.628-5205G>T	ENSP00000385669.3:n.628-5205G>T
ENST00000547718.5:c.*585-5205G>T	ENSP00000447294.1:n.*585-5205G>T
ENST00000622220.1:c.358-5205G>T	ENSP00000483051.1:n.358-5205G>T
NM_001109903.1:c.628-5205G>T	NP_001103373.1:n.628-5205G>T
NM_032814.3:c.628-5205G>T	NP_116203.2:n.628-5205G>T
XM_005253969.2:c.628-5205G>T	XP_005254026.1:n.628-5205G>T
XM_011538895.1:c.628-5205G>T	XP_011537197.1:n.628-5205G>T
XM_011538896.1:c.628-5205G>T	XP_011537198.1:n.628-5205G>T
XM_011538897.1:c.628-5205G>T	XP_011537199.1:n.628-5205G>T
XR_001748905.2:n.837-5205G>T
NM_032814.4:c.628-5205G>T	NP_116203.2:n.628-5205G>T
NM_001109903.2:c.628-5205G>T	NP_001103373.1:n.628-5205G>T
NM_001382266.1:c.628-5205G>T MANE Select	NP_001369195.1:n.628-5205G>T