Canonical Allele Identifier: CA2485643497
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664978791

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883651del , CM000663.2:g.212883651del GRCh38
NC_000001.10:g.213056993del , CM000663.1:g.213056993del GRCh37
NC_000001.9:g.211123616del NCBI36
NG_028131.1:g.30397del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+213del MANE Select ENSP00000355938.4:n.1092+213del
ENST00000366971.8:c.1092+213del ENSP00000355938.4:n.1092+213del
ENST00000419102.1:c.488+213del
ENST00000474693.1:n.317+213del
ENST00000483790.1:n.30+213del
NM_014053.3:c.1092+213del NP_054772.1:n.1092+213del
XM_011509446.1:c.1092+213del XP_011507748.1:n.1092+213del
XR_247024.1:n.1266+213del
XR_426771.1:n.1393+213del
XM_011509446.3:c.1092+213del XP_011507748.1:n.1092+213del
XR_247024.3:n.1266+213del
NM_014053.4:c.1092+213del MANE Select NP_054772.1:n.1092+213del