Canonical Allele Identifier: CA9322797

Gene: RFXANK

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19198208C>T , CM000681.2:g.19198208C>T	GRCh38
NC_000019.9:g.19309017C>T , CM000681.1:g.19309017C>T	GRCh37
NC_000019.8:g.19170017C>T	NCBI36
NG_007432.1:g.11010C>T , LRG_102:g.11010C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003721.4:c.540C>T MANE Select	NP_003712.1:p.Asp180=
ENST00000303088.9:c.540C>T MANE Select	ENSP00000305071.2:p.Asp180=
NM_001278727.1:c.474C>T	NP_001265656.1:p.Asp158=
NM_001278727.2:c.474C>T	NP_001265656.1:p.Asp158=
NM_001278728.1:c.471C>T	NP_001265657.1:p.Asp157=
NM_001278728.2:c.471C>T	NP_001265657.1:p.Asp157=
NM_001370233.1:c.540C>T	NP_001357162.1:p.Asp180=
NM_001370234.1:c.474C>T	NP_001357163.1:p.Asp158=
NM_001370235.1:c.537C>T	NP_001357164.1:p.Asp179=
NM_001370236.1:c.537C>T	NP_001357165.1:p.Asp179=
NM_001370237.1:c.537C>T	NP_001357166.1:p.Asp179=
NM_001370238.1:c.540C>T	NP_001357167.1:p.Asp180=
NM_003721.3:c.540C>T	NP_003712.1:p.Asp180=
NM_134440.2:c.471C>T	NP_604389.1:p.Asp157=
NM_134440.3:c.471C>T	NP_604389.1:p.Asp157=
ENST00000303088.8:c.540C>T	ENSP00000305071.2:p.Asp180=
ENST00000392324.8:c.471C>T	ENSP00000376138.3:p.Asp157=
ENST00000407360.7:c.540C>T	ENSP00000384572.3:p.Asp180=
ENST00000456252.7:c.474C>T	ENSP00000409138.2:p.Asp158=
ENST00000535017.1:c.369C>T	ENSP00000444280.1:p.Asp123=
ENST00000540981.5:c.474C>T	ENSP00000440325.2:p.Asp158=
ENST00000541873.6:n.733C>T
XM_005260134.3:c.540C>T	XP_005260191.1:p.Asp180=
XM_005260134.5:c.540C>T	XP_005260191.1:p.Asp180=
XM_005260135.2:c.540C>T	XP_005260192.1:p.Asp180=
XM_005260135.3:c.540C>T	XP_005260192.1:p.Asp180=
XM_005260136.3:c.537C>T	XP_005260193.1:p.Asp179=
XM_005260136.5:c.537C>T	XP_005260193.1:p.Asp179=
XM_005260137.3:c.537C>T	XP_005260194.1:p.Asp179=
XM_005260137.4:c.537C>T	XP_005260194.1:p.Asp179=
XM_006722930.2:c.537C>T	XP_006722993.1:p.Asp179=
XM_006722930.4:c.537C>T	XP_006722993.1:p.Asp179=
XM_017027415.1:c.540C>T	XP_016882904.1:p.Asp180=
XM_017027416.1:c.474C>T	XP_016882905.1:p.Asp158=