Canonical Allele Identifier: CA2485643543
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664984052

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883770_212883778del , CM000663.2:g.212883770_212883778del GRCh38
NC_000001.10:g.213057112_213057120del , CM000663.1:g.213057112_213057120del GRCh37
NC_000001.9:g.211123735_211123743del NCBI36
NG_028131.1:g.30516_30524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+332_1092+340del MANE Select ENSP00000355938.4:n.1092+332_1092+340del
ENST00000366971.8:c.1092+332_1092+340del ENSP00000355938.4:n.1092+332_1092+340del
ENST00000419102.1:c.488+332_488+340del
ENST00000474693.1:n.317+332_317+340del
ENST00000483790.1:n.30+332_30+340del
NM_014053.3:c.1092+332_1092+340del NP_054772.1:n.1092+332_1092+340del
XM_011509446.1:c.1092+332_1092+340del XP_011507748.1:n.1092+332_1092+340del
XR_247024.1:n.1266+332_1266+340del
XR_426771.1:n.1393+332_1393+340del
XM_011509446.3:c.1092+332_1092+340del XP_011507748.1:n.1092+332_1092+340del
XR_247024.3:n.1266+332_1266+340del
NM_014053.4:c.1092+332_1092+340del MANE Select NP_054772.1:n.1092+332_1092+340del