Canonical Allele Identifier: CA16603563
Gene: FLVCR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 379610
ClinVar RCV Id: RCV000434937
dbSNP Id: rs1057520666

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212885292G>A , CM000663.2:g.212885292G>A GRCh38
NC_000001.10:g.213058634G>A , CM000663.1:g.213058634G>A GRCh37
NC_000001.9:g.211125257G>A NCBI36
NG_028131.1:g.32038G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366971.9:c.1093-1G>A MANE Select ENSP00000355938.4:n.1093-1G>A
ENST00000366971.8:c.1093-1G>A ENSP00000355938.4:n.1093-1G>A
ENST00000419102.1:c.489-1G>A
ENST00000474693.1:n.318-1G>A
ENST00000483790.1:n.31-1G>A
NM_014053.3:c.1093-1G>A NP_054772.1:n.1093-1G>A
XM_011509446.1:c.1093-1G>A XP_011507748.1:n.1093-1G>A
XR_247024.1:n.1267-1G>A
XR_426771.1:n.1394-1G>A
XM_011509446.3:c.1093-1G>A XP_011507748.1:n.1093-1G>A
XR_247024.3:n.1267-1G>A
NM_014053.4:c.1093-1G>A MANE Select NP_054772.1:n.1093-1G>A