Canonical Allele Identifier: CA2747647716
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883582_212883583insA , CM000663.2:g.212883582_212883583insA GRCh38
NC_000001.10:g.213056924_213056925insA , CM000663.1:g.213056924_213056925insA GRCh37
NC_000001.9:g.211123547_211123548insA NCBI36
NG_028131.1:g.30328_30329insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+144_1092+145insA MANE Select ENSP00000355938.4:n.1092+144_1092+145insA
ENST00000366971.8:c.1092+144_1092+145insA ENSP00000355938.4:n.1092+144_1092+145insA
ENST00000419102.1:c.488+144_488+145insA
ENST00000474693.1:n.317+144_317+145insA
ENST00000483790.1:n.30+144_30+145insA
NM_014053.3:c.1092+144_1092+145insA NP_054772.1:n.1092+144_1092+145insA
XM_011509446.1:c.1092+144_1092+145insA XP_011507748.1:n.1092+144_1092+145insA
XR_247024.1:n.1266+144_1266+145insA
XR_426771.1:n.1393+144_1393+145insA
XM_011509446.3:c.1092+144_1092+145insA XP_011507748.1:n.1092+144_1092+145insA
XR_247024.3:n.1266+144_1266+145insA
NM_014053.4:c.1092+144_1092+145insA MANE Select NP_054772.1:n.1092+144_1092+145insA