Canonical Allele Identifier: CA1148300392
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883435T= , CM000663.2:g.212883435T= GRCh38
NC_000001.10:g.213056777T= , CM000663.1:g.213056777T= GRCh37
NC_000001.9:g.211123400T= NCBI36
NG_028131.1:g.30181T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1089T= MANE Select ENSP00000355938.4:p.Tyr363=
ENST00000366971.8:c.1089T= ENSP00000355938.4:p.Tyr363=
ENST00000419102.1:c.485T=
ENST00000474693.1:n.314T=
ENST00000483790.1:n.27T=
NM_014053.3:c.1089T= NP_054772.1:p.Tyr363=
XM_011509446.1:c.1089T= XP_011507748.1:p.Tyr363=
XR_247024.1:n.1263T=
XR_426771.1:n.1390T=
XM_011509446.3:c.1089T= XP_011507748.1:p.Tyr363=
XR_247024.3:n.1263T=
NM_014053.4:c.1089T= MANE Select NP_054772.1:p.Tyr363=