Canonical Allele Identifier: CA1012018036
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664973687

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883452T>G , CM000663.2:g.212883452T>G GRCh38
NC_000001.10:g.213056794T>G , CM000663.1:g.213056794T>G GRCh37
NC_000001.9:g.211123417T>G NCBI36
NG_028131.1:g.30198T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+14T>G MANE Select ENSP00000355938.4:n.1092+14T>G
ENST00000366971.8:c.1092+14T>G ENSP00000355938.4:n.1092+14T>G
ENST00000419102.1:c.488+14T>G
ENST00000474693.1:n.317+14T>G
ENST00000483790.1:n.30+14T>G
NM_014053.3:c.1092+14T>G NP_054772.1:n.1092+14T>G
XM_011509446.1:c.1092+14T>G XP_011507748.1:n.1092+14T>G
XR_247024.1:n.1266+14T>G
XR_426771.1:n.1393+14T>G
XM_011509446.3:c.1092+14T>G XP_011507748.1:n.1092+14T>G
XR_247024.3:n.1266+14T>G
NM_014053.4:c.1092+14T>G MANE Select NP_054772.1:n.1092+14T>G