Canonical Allele Identifier: CA2747647695
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883527_212883528insA , CM000663.2:g.212883527_212883528insA GRCh38
NC_000001.10:g.213056869_213056870insA , CM000663.1:g.213056869_213056870insA GRCh37
NC_000001.9:g.211123492_211123493insA NCBI36
NG_028131.1:g.30273_30274insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+89_1092+90insA MANE Select ENSP00000355938.4:n.1092+89_1092+90insA
ENST00000366971.8:c.1092+89_1092+90insA ENSP00000355938.4:n.1092+89_1092+90insA
ENST00000419102.1:c.488+89_488+90insA
ENST00000474693.1:n.317+89_317+90insA
ENST00000483790.1:n.30+89_30+90insA
NM_014053.3:c.1092+89_1092+90insA NP_054772.1:n.1092+89_1092+90insA
XM_011509446.1:c.1092+89_1092+90insA XP_011507748.1:n.1092+89_1092+90insA
XR_247024.1:n.1266+89_1266+90insA
XR_426771.1:n.1393+89_1393+90insA
XM_011509446.3:c.1092+89_1092+90insA XP_011507748.1:n.1092+89_1092+90insA
XR_247024.3:n.1266+89_1266+90insA
NM_014053.4:c.1092+89_1092+90insA MANE Select NP_054772.1:n.1092+89_1092+90insA