Canonical Allele Identifier: CA2518121529
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883638_212883639insAAAA , CM000663.2:g.212883638_212883639insAAAA GRCh38
NC_000001.10:g.213056980_213056981insAAAA , CM000663.1:g.213056980_213056981insAAAA GRCh37
NC_000001.9:g.211123603_211123604insAAAA NCBI36
NG_028131.1:g.30384_30385insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+200_1092+201insAAAA MANE Select ENSP00000355938.4:n.1092+200_1092+201insAAAA
ENST00000366971.8:c.1092+200_1092+201insAAAA ENSP00000355938.4:n.1092+200_1092+201insAAAA
ENST00000419102.1:c.488+200_488+201insAAAA
ENST00000474693.1:n.317+200_317+201insAAAA
ENST00000483790.1:n.30+200_30+201insAAAA
NM_014053.3:c.1092+200_1092+201insAAAA NP_054772.1:n.1092+200_1092+201insAAAA
XM_011509446.1:c.1092+200_1092+201insAAAA XP_011507748.1:n.1092+200_1092+201insAAAA
XR_247024.1:n.1266+200_1266+201insAAAA
XR_426771.1:n.1393+200_1393+201insAAAA
XM_011509446.3:c.1092+200_1092+201insAAAA XP_011507748.1:n.1092+200_1092+201insAAAA
XR_247024.3:n.1266+200_1266+201insAAAA
NM_014053.4:c.1092+200_1092+201insAAAA MANE Select NP_054772.1:n.1092+200_1092+201insAAAA