Canonical Allele Identifier: CA1012017969
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664970179

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883344_212883381del , CM000663.2:g.212883344_212883381del GRCh38
NC_000001.10:g.213056686_213056723del , CM000663.1:g.213056686_213056723del GRCh37
NC_000001.9:g.211123309_211123346del NCBI36
NG_028131.1:g.30090_30127del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-27_1035del
ENST00000366971.8:c.1025-27_1035del
ENST00000419102.1:c.421-27_431del
ENST00000474693.1:n.250-27_260del
NM_014053.3:c.1025-27_1035del
XM_011509446.1:c.1025-27_1035del
XR_247024.1:n.1199-27_1209del
XR_426771.1:n.1326-27_1336del
XM_011509446.3:c.1025-27_1035del
XR_247024.3:n.1199-27_1209del
NM_014053.4:c.1025-27_1035del