Canonical Allele Identifier: CA2485643542
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883769_212883778delinsCAAAGTTACT , CM000663.2:g.212883769_212883778delinsCAAAGTTACT GRCh38
NC_000001.10:g.213057111_213057120delinsCAAAGTTACT , CM000663.1:g.213057111_213057120delinsCAAAGTTACT GRCh37
NC_000001.9:g.211123734_211123743delinsCAAAGTTACT NCBI36
NG_028131.1:g.30515_30524delinsCAAAGTTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+331_1092+340delinsCAAAGTTACT MANE Select ENSP00000355938.4:n.1092+331_1092+340delinsCAAAGTTACT
ENST00000366971.8:c.1092+331_1092+340delinsCAAAGTTACT ENSP00000355938.4:n.1092+331_1092+340delinsCAAAGTTACT
ENST00000419102.1:c.488+331_488+340delinsCAAAGTTACT
ENST00000474693.1:n.317+331_317+340delinsCAAAGTTACT
ENST00000483790.1:n.30+331_30+340delinsCAAAGTTACT
NM_014053.3:c.1092+331_1092+340delinsCAAAGTTACT NP_054772.1:n.1092+331_1092+340delinsCAAAGTTACT
XM_011509446.1:c.1092+331_1092+340delinsCAAAGTTACT XP_011507748.1:n.1092+331_1092+340delinsCAAAGTTACT
XR_247024.1:n.1266+331_1266+340delinsCAAAGTTACT
XR_426771.1:n.1393+331_1393+340delinsCAAAGTTACT
XM_011509446.3:c.1092+331_1092+340delinsCAAAGTTACT XP_011507748.1:n.1092+331_1092+340delinsCAAAGTTACT
XR_247024.3:n.1266+331_1266+340delinsCAAAGTTACT
NM_014053.4:c.1092+331_1092+340delinsCAAAGTTACT MANE Select NP_054772.1:n.1092+331_1092+340delinsCAAAGTTACT