Canonical Allele Identifier: CA2485643333
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664968884

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883227_212883239del , CM000663.2:g.212883227_212883239del GRCh38
NC_000001.10:g.213056569_213056581del , CM000663.1:g.213056569_213056581del GRCh37
NC_000001.9:g.211123192_211123204del NCBI36
NG_028131.1:g.29973_29985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-144_1025-132del MANE Select ENSP00000355938.4:n.1025-144_1025-132del
ENST00000366971.8:c.1025-144_1025-132del ENSP00000355938.4:n.1025-144_1025-132del
ENST00000419102.1:c.421-144_421-132del
ENST00000474693.1:n.250-144_250-132del
NM_014053.3:c.1025-144_1025-132del NP_054772.1:n.1025-144_1025-132del
XM_011509446.1:c.1025-144_1025-132del XP_011507748.1:n.1025-144_1025-132del
XR_247024.1:n.1199-144_1199-132del
XR_426771.1:n.1326-144_1326-132del
XM_011509446.3:c.1025-144_1025-132del XP_011507748.1:n.1025-144_1025-132del
XR_247024.3:n.1199-144_1199-132del
NM_014053.4:c.1025-144_1025-132del MANE Select NP_054772.1:n.1025-144_1025-132del