Canonical Allele Identifier: CA2485633259
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212858821T= , CM000663.2:g.212858821T= GRCh38
NC_000001.10:g.213032163T= , CM000663.1:g.213032163T= GRCh37
NC_000001.9:g.211098786T= NCBI36
NG_028131.1:g.5567T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.369T= MANE Select ENSP00000355938.4:p.Phe123=
ENST00000366971.8:c.369T= ENSP00000355938.4:p.Phe123=
NM_014053.3:c.369T= NP_054772.1:p.Phe123=
XM_011509446.1:c.369T= XP_011507748.1:p.Phe123=
XM_011509447.1:c.369T= XP_011507749.1:p.Phe123=
XM_011509448.1:c.369T= XP_011507750.1:p.Phe123=
XR_247024.1:n.543T=
XR_426771.1:n.543T=
XR_426772.2:n.543T=
XR_921769.1:n.543T=
XM_011509446.3:c.369T= XP_011507748.1:p.Phe123=
XM_011509447.2:c.369T= XP_011507749.1:p.Phe123=
XR_247024.3:n.543T=
XR_426772.3:n.543T=
NM_014053.4:c.369T= MANE Select NP_054772.1:p.Phe123=