Canonical Allele Identifier: CA404894518

Gene: RFXANK

Linked Data

• gnomAD v4: 19-19197550-C-G
• MyVariant Identifiers: chr19:g.19308359C>G (hg19) ; chr19:g.19197550C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19197550C>G , CM000681.2:g.19197550C>G	GRCh38
NC_000019.9:g.19308359C>G , CM000681.1:g.19308359C>G	GRCh37
NC_000019.8:g.19169359C>G	NCBI36
NG_007432.1:g.10352C>G , LRG_102:g.10352C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000303088.9:c.367C>G MANE Select	ENSP00000305071.2:p.Arg123Gly
ENST00000303088.8:c.367C>G	ENSP00000305071.2:p.Arg123Gly
ENST00000392324.8:c.298C>G	ENSP00000376138.3:p.Arg100Gly
ENST00000407360.7:c.367C>G	ENSP00000384572.3:p.Arg123Gly
ENST00000456252.7:c.301C>G	ENSP00000409138.2:p.Arg101Gly
ENST00000535017.1:c.196C>G	ENSP00000444280.1:p.Arg66Gly
ENST00000540981.5:c.301C>G	ENSP00000440325.2:p.Arg101Gly
ENST00000541873.6:n.560C>G
ENST00000543118.1:n.296C>G
ENST00000545522.2:n.775C>G
ENST00000593273.5:c.364C>G	ENSP00000466913.1:p.Arg122Gly
NM_001278727.1:c.301C>G	NP_001265656.1:p.Arg101Gly
NM_001278728.1:c.298C>G	NP_001265657.1:p.Arg100Gly
NM_003721.3:c.367C>G	NP_003712.1:p.Arg123Gly
NM_134440.2:c.298C>G	NP_604389.1:p.Arg100Gly
XM_005260134.3:c.367C>G	XP_005260191.1:p.Arg123Gly
XM_005260135.2:c.367C>G	XP_005260192.1:p.Arg123Gly
XM_005260136.3:c.364C>G	XP_005260193.1:p.Arg122Gly
XM_005260137.3:c.364C>G	XP_005260194.1:p.Arg122Gly
XM_006722930.2:c.364C>G	XP_006722993.1:p.Arg122Gly
XM_005260134.5:c.367C>G	XP_005260191.1:p.Arg123Gly
XM_005260135.3:c.367C>G	XP_005260192.1:p.Arg123Gly
XM_005260136.5:c.364C>G	XP_005260193.1:p.Arg122Gly
XM_005260137.4:c.364C>G	XP_005260194.1:p.Arg122Gly
XM_006722930.4:c.364C>G	XP_006722993.1:p.Arg122Gly
XM_017027415.1:c.367C>G	XP_016882904.1:p.Arg123Gly
XM_017027416.1:c.301C>G	XP_016882905.1:p.Arg101Gly
NM_003721.4:c.367C>G MANE Select	NP_003712.1:p.Arg123Gly
NM_001370233.1:c.367C>G	NP_001357162.1:p.Arg123Gly
NM_001370234.1:c.301C>G	NP_001357163.1:p.Arg101Gly
NM_001370235.1:c.364C>G	NP_001357164.1:p.Arg122Gly
NM_001370236.1:c.364C>G	NP_001357165.1:p.Arg122Gly
NM_001370237.1:c.364C>G	NP_001357166.1:p.Arg122Gly
NM_001370238.1:c.367C>G	NP_001357167.1:p.Arg123Gly
NM_001278727.2:c.301C>G	NP_001265656.1:p.Arg101Gly
NM_001278728.2:c.298C>G	NP_001265657.1:p.Arg100Gly
NM_134440.3:c.298C>G	NP_604389.1:p.Arg100Gly