Canonical Allele Identifier: CA9322706
Gene: RFXANK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19197496_19197521del , CM000681.2:g.19197496_19197521del GRCh38
NC_000019.9:g.19308305_19308330del , CM000681.1:g.19308305_19308330del GRCh37
NC_000019.8:g.19169305_19169330del NCBI36
NG_007432.1:g.10298_10323del , LRG_102:g.10298_10323del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303088.9:c.338-25_338del
ENST00000303088.8:c.338-25_338del
ENST00000392324.8:c.269-25_269del
ENST00000407360.7:c.338-25_338del
ENST00000456252.7:c.272-25_272del
ENST00000535017.1:c.167-25_167del
ENST00000540981.5:c.272-25_272del
ENST00000541873.6:n.531-25_531del
ENST00000543118.1:n.242_267del
ENST00000545522.2:n.721_746del
ENST00000593273.5:c.335-25_335del
NM_001278727.1:c.272-25_272del
NM_001278728.1:c.269-25_269del
NM_003721.3:c.338-25_338del
NM_134440.2:c.269-25_269del
XM_005260134.3:c.338-25_338del
XM_005260135.2:c.338-25_338del
XM_005260136.3:c.335-25_335del
XM_005260137.3:c.335-25_335del
XM_006722930.2:c.335-25_335del
XM_005260134.5:c.338-25_338del
XM_005260135.3:c.338-25_338del
XM_005260136.5:c.335-25_335del
XM_005260137.4:c.335-25_335del
XM_006722930.4:c.335-25_335del
XM_017027415.1:c.338-25_338del
XM_017027416.1:c.272-25_272del
NM_003721.4:c.338-25_338del
NM_001370233.1:c.338-25_338del
NM_001370234.1:c.272-25_272del
NM_001370235.1:c.335-25_335del
NM_001370236.1:c.335-25_335del
NM_001370237.1:c.335-25_335del
NM_001370238.1:c.338-25_338del
NM_001278727.2:c.272-25_272del
NM_001278728.2:c.269-25_269del
NM_134440.3:c.269-25_269del