Canonical Allele Identifier: CA2485643511
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664981536

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883698_212883700del , CM000663.2:g.212883698_212883700del GRCh38
NC_000001.10:g.213057040_213057042del , CM000663.1:g.213057040_213057042del GRCh37
NC_000001.9:g.211123663_211123665del NCBI36
NG_028131.1:g.30444_30446del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+260_1092+262del MANE Select ENSP00000355938.4:n.1092+260_1092+262del
ENST00000366971.8:c.1092+260_1092+262del ENSP00000355938.4:n.1092+260_1092+262del
ENST00000419102.1:c.488+260_488+262del
ENST00000474693.1:n.317+260_317+262del
ENST00000483790.1:n.30+260_30+262del
NM_014053.3:c.1092+260_1092+262del NP_054772.1:n.1092+260_1092+262del
XM_011509446.1:c.1092+260_1092+262del XP_011507748.1:n.1092+260_1092+262del
XR_247024.1:n.1266+260_1266+262del
XR_426771.1:n.1393+260_1393+262del
XM_011509446.3:c.1092+260_1092+262del XP_011507748.1:n.1092+260_1092+262del
XR_247024.3:n.1266+260_1266+262del
NM_014053.4:c.1092+260_1092+262del MANE Select NP_054772.1:n.1092+260_1092+262del