Canonical Allele Identifier: CA2583682354

Gene: RFXANK

Linked Data

• gnomAD v4: 19-19197406-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19197406_19197407insAT , CM000681.2:g.19197406_19197407insAT	GRCh38
NC_000019.9:g.19308215_19308216insAT , CM000681.1:g.19308215_19308216insAT	GRCh37
NC_000019.8:g.19169215_19169216insAT	NCBI36
NG_007432.1:g.10208_10209insAT , LRG_102:g.10208_10209insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303088.9:c.338-115_338-114insAT MANE Select	ENSP00000305071.2:n.338-115_338-114insAT
ENST00000303088.8:c.338-115_338-114insAT	ENSP00000305071.2:n.338-115_338-114insAT
ENST00000392324.8:c.269-115_269-114insAT	ENSP00000376138.3:n.269-115_269-114insAT
ENST00000407360.7:c.338-115_338-114insAT	ENSP00000384572.3:n.338-115_338-114insAT
ENST00000456252.7:c.272-115_272-114insAT	ENSP00000409138.2:n.272-115_272-114insAT
ENST00000535017.1:c.167-115_167-114insAT	ENSP00000444280.1:n.167-115_167-114insAT
ENST00000540981.5:c.272-115_272-114insAT	ENSP00000440325.2:n.272-115_272-114insAT
ENST00000541873.6:n.531-115_531-114insAT
ENST00000543118.1:n.152_153insAT
ENST00000543157.7:n.891_892insAT
ENST00000545522.2:n.631_632insAT
ENST00000593273.5:c.335-115_335-114insAT	ENSP00000466913.1:n.335-115_335-114insAT
NM_001278727.1:c.272-115_272-114insAT	NP_001265656.1:n.272-115_272-114insAT
NM_001278728.1:c.269-115_269-114insAT	NP_001265657.1:n.269-115_269-114insAT
NM_003721.3:c.338-115_338-114insAT	NP_003712.1:n.338-115_338-114insAT
NM_134440.2:c.269-115_269-114insAT	NP_604389.1:n.269-115_269-114insAT
XM_005260134.3:c.338-115_338-114insAT	XP_005260191.1:n.338-115_338-114insAT
XM_005260135.2:c.338-115_338-114insAT	XP_005260192.1:n.338-115_338-114insAT
XM_005260136.3:c.335-115_335-114insAT	XP_005260193.1:n.335-115_335-114insAT
XM_005260137.3:c.335-115_335-114insAT	XP_005260194.1:n.335-115_335-114insAT
XM_006722930.2:c.335-115_335-114insAT	XP_006722993.1:n.335-115_335-114insAT
XM_005260134.5:c.338-115_338-114insAT	XP_005260191.1:n.338-115_338-114insAT
XM_005260135.3:c.338-115_338-114insAT	XP_005260192.1:n.338-115_338-114insAT
XM_005260136.5:c.335-115_335-114insAT	XP_005260193.1:n.335-115_335-114insAT
XM_005260137.4:c.335-115_335-114insAT	XP_005260194.1:n.335-115_335-114insAT
XM_006722930.4:c.335-115_335-114insAT	XP_006722993.1:n.335-115_335-114insAT
XM_017027415.1:c.338-115_338-114insAT	XP_016882904.1:n.338-115_338-114insAT
XM_017027416.1:c.272-115_272-114insAT	XP_016882905.1:n.272-115_272-114insAT
NM_003721.4:c.338-115_338-114insAT MANE Select	NP_003712.1:n.338-115_338-114insAT
NM_001370233.1:c.338-115_338-114insAT	NP_001357162.1:n.338-115_338-114insAT
NM_001370234.1:c.272-115_272-114insAT	NP_001357163.1:n.272-115_272-114insAT
NM_001370235.1:c.335-115_335-114insAT	NP_001357164.1:n.335-115_335-114insAT
NM_001370236.1:c.335-115_335-114insAT	NP_001357165.1:n.335-115_335-114insAT
NM_001370237.1:c.335-115_335-114insAT	NP_001357166.1:n.335-115_335-114insAT
NM_001370238.1:c.338-115_338-114insAT	NP_001357167.1:n.338-115_338-114insAT
NM_001278727.2:c.272-115_272-114insAT	NP_001265656.1:n.272-115_272-114insAT
NM_001278728.2:c.269-115_269-114insAT	NP_001265657.1:n.269-115_269-114insAT
NM_134440.3:c.269-115_269-114insAT	NP_604389.1:n.269-115_269-114insAT