Canonical Allele Identifier: CA2485643518
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883717_212883718delinsGA , CM000663.2:g.212883717_212883718delinsGA GRCh38
NC_000001.10:g.213057059_213057060delinsGA , CM000663.1:g.213057059_213057060delinsGA GRCh37
NC_000001.9:g.211123682_211123683delinsGA NCBI36
NG_028131.1:g.30463_30464delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+279_1092+280delinsGA MANE Select ENSP00000355938.4:n.1092+279_1092+280delinsGA
ENST00000366971.8:c.1092+279_1092+280delinsGA ENSP00000355938.4:n.1092+279_1092+280delinsGA
ENST00000419102.1:c.488+279_488+280delinsGA
ENST00000474693.1:n.317+279_317+280delinsGA
ENST00000483790.1:n.30+279_30+280delinsGA
NM_014053.3:c.1092+279_1092+280delinsGA NP_054772.1:n.1092+279_1092+280delinsGA
XM_011509446.1:c.1092+279_1092+280delinsGA XP_011507748.1:n.1092+279_1092+280delinsGA
XR_247024.1:n.1266+279_1266+280delinsGA
XR_426771.1:n.1393+279_1393+280delinsGA
XM_011509446.3:c.1092+279_1092+280delinsGA XP_011507748.1:n.1092+279_1092+280delinsGA
XR_247024.3:n.1266+279_1266+280delinsGA
NM_014053.4:c.1092+279_1092+280delinsGA MANE Select NP_054772.1:n.1092+279_1092+280delinsGA