Canonical Allele Identifier: CA1012017987
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664970741

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883343_212883344del , CM000663.2:g.212883343_212883344del GRCh38
NC_000001.10:g.213056685_213056686del , CM000663.1:g.213056685_213056686del GRCh37
NC_000001.9:g.211123308_211123309del NCBI36
NG_028131.1:g.30089_30090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-28_1025-27del MANE Select ENSP00000355938.4:n.1025-28_1025-27del
ENST00000366971.8:c.1025-28_1025-27del ENSP00000355938.4:n.1025-28_1025-27del
ENST00000419102.1:c.421-28_421-27del
ENST00000474693.1:n.250-28_250-27del
NM_014053.3:c.1025-28_1025-27del NP_054772.1:n.1025-28_1025-27del
XM_011509446.1:c.1025-28_1025-27del XP_011507748.1:n.1025-28_1025-27del
XR_247024.1:n.1199-28_1199-27del
XR_426771.1:n.1326-28_1326-27del
XM_011509446.3:c.1025-28_1025-27del XP_011507748.1:n.1025-28_1025-27del
XR_247024.3:n.1199-28_1199-27del
NM_014053.4:c.1025-28_1025-27del MANE Select NP_054772.1:n.1025-28_1025-27del