Canonical Allele Identifier: CA2326726707
Gene: RFXANK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19197545A= , CM000681.2:g.19197545A= GRCh38
NC_000019.9:g.19308354A= , CM000681.1:g.19308354A= GRCh37
NC_000019.8:g.19169354A= NCBI36
NG_007432.1:g.10347A= , LRG_102:g.10347A=

Transcript Alleles

HGVS Amino-acid Change
NM_003721.4:c.362A= MANE Select NP_003712.1:p.Asp121=
ENST00000303088.9:c.362A= MANE Select ENSP00000305071.2:p.Asp121=
NM_001278727.1:c.296A= NP_001265656.1:p.Asp99=
NM_001278727.2:c.296A= NP_001265656.1:p.Asp99=
NM_001278728.1:c.293A= NP_001265657.1:p.Asp98=
NM_001278728.2:c.293A= NP_001265657.1:p.Asp98=
NM_001370233.1:c.362A= NP_001357162.1:p.Asp121=
NM_001370234.1:c.296A= NP_001357163.1:p.Asp99=
NM_001370235.1:c.359A= NP_001357164.1:p.Asp120=
NM_001370236.1:c.359A= NP_001357165.1:p.Asp120=
NM_001370237.1:c.359A= NP_001357166.1:p.Asp120=
NM_001370238.1:c.362A= NP_001357167.1:p.Asp121=
NM_003721.3:c.362A= NP_003712.1:p.Asp121=
NM_134440.2:c.293A= NP_604389.1:p.Asp98=
NM_134440.3:c.293A= NP_604389.1:p.Asp98=
ENST00000303088.8:c.362A= ENSP00000305071.2:p.Asp121=
ENST00000392324.8:c.293A= ENSP00000376138.3:p.Asp98=
ENST00000407360.7:c.362A= ENSP00000384572.3:p.Asp121=
ENST00000456252.7:c.296A= ENSP00000409138.2:p.Asp99=
ENST00000535017.1:c.191A= ENSP00000444280.1:p.Asp64=
ENST00000540981.5:c.296A= ENSP00000440325.2:p.Asp99=
ENST00000541873.6:n.555A=
ENST00000543118.1:n.291A=
ENST00000545522.2:n.770A=
ENST00000593273.5:c.359A= ENSP00000466913.1:p.Asp120=
XM_005260134.3:c.362A= XP_005260191.1:p.Asp121=
XM_005260134.5:c.362A= XP_005260191.1:p.Asp121=
XM_005260135.2:c.362A= XP_005260192.1:p.Asp121=
XM_005260135.3:c.362A= XP_005260192.1:p.Asp121=
XM_005260136.3:c.359A= XP_005260193.1:p.Asp120=
XM_005260136.5:c.359A= XP_005260193.1:p.Asp120=
XM_005260137.3:c.359A= XP_005260194.1:p.Asp120=
XM_005260137.4:c.359A= XP_005260194.1:p.Asp120=
XM_006722930.2:c.359A= XP_006722993.1:p.Asp120=
XM_006722930.4:c.359A= XP_006722993.1:p.Asp120=
XM_017027415.1:c.362A= XP_016882904.1:p.Asp121=
XM_017027416.1:c.296A= XP_016882905.1:p.Asp99=