Canonical Allele Identifier: CA2485643474
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883602_212883603delinsAC , CM000663.2:g.212883602_212883603delinsAC GRCh38
NC_000001.10:g.213056944_213056945delinsAC , CM000663.1:g.213056944_213056945delinsAC GRCh37
NC_000001.9:g.211123567_211123568delinsAC NCBI36
NG_028131.1:g.30348_30349delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+164_1092+165delinsAC MANE Select ENSP00000355938.4:n.1092+164_1092+165delinsAC
ENST00000366971.8:c.1092+164_1092+165delinsAC ENSP00000355938.4:n.1092+164_1092+165delinsAC
ENST00000419102.1:c.488+164_488+165delinsAC
ENST00000474693.1:n.317+164_317+165delinsAC
ENST00000483790.1:n.30+164_30+165delinsAC
NM_014053.3:c.1092+164_1092+165delinsAC NP_054772.1:n.1092+164_1092+165delinsAC
XM_011509446.1:c.1092+164_1092+165delinsAC XP_011507748.1:n.1092+164_1092+165delinsAC
XR_247024.1:n.1266+164_1266+165delinsAC
XR_426771.1:n.1393+164_1393+165delinsAC
XM_011509446.3:c.1092+164_1092+165delinsAC XP_011507748.1:n.1092+164_1092+165delinsAC
XR_247024.3:n.1266+164_1266+165delinsAC
NM_014053.4:c.1092+164_1092+165delinsAC MANE Select NP_054772.1:n.1092+164_1092+165delinsAC