Canonical Allele Identifier: CA1143881382
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883404C= , CM000663.2:g.212883404C= GRCh38
NC_000001.10:g.213056746C= , CM000663.1:g.213056746C= GRCh37
NC_000001.9:g.211123369C= NCBI36
NG_028131.1:g.30150C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1058C= MANE Select ENSP00000355938.4:p.Thr353=
ENST00000366971.8:c.1058C= ENSP00000355938.4:p.Thr353=
ENST00000419102.1:c.454C=
ENST00000474693.1:n.283C=
NM_014053.3:c.1058C= NP_054772.1:p.Thr353=
XM_011509446.1:c.1058C= XP_011507748.1:p.Thr353=
XR_247024.1:n.1232C=
XR_426771.1:n.1359C=
XM_011509446.3:c.1058C= XP_011507748.1:p.Thr353=
XR_247024.3:n.1232C=
NM_014053.4:c.1058C= MANE Select NP_054772.1:p.Thr353=