Canonical Allele Identifier: CA2485643294
Gene: FLVCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883111_212883112delinsAT , CM000663.2:g.212883111_212883112delinsAT GRCh38
NC_000001.10:g.213056453_213056454delinsAT , CM000663.1:g.213056453_213056454delinsAT GRCh37
NC_000001.9:g.211123076_211123077delinsAT NCBI36
NG_028131.1:g.29857_29858delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-260_1025-259delinsAT MANE Select ENSP00000355938.4:n.1025-260_1025-259delinsAT
ENST00000366971.8:c.1025-260_1025-259delinsAT ENSP00000355938.4:n.1025-260_1025-259delinsAT
ENST00000419102.1:c.421-260_421-259delinsAT
ENST00000474693.1:n.250-260_250-259delinsAT
NM_014053.3:c.1025-260_1025-259delinsAT NP_054772.1:n.1025-260_1025-259delinsAT
XM_011509446.1:c.1025-260_1025-259delinsAT XP_011507748.1:n.1025-260_1025-259delinsAT
XR_247024.1:n.1199-260_1199-259delinsAT
XR_426771.1:n.1326-260_1326-259delinsAT
XM_011509446.3:c.1025-260_1025-259delinsAT XP_011507748.1:n.1025-260_1025-259delinsAT
XR_247024.3:n.1199-260_1199-259delinsAT
NM_014053.4:c.1025-260_1025-259delinsAT MANE Select NP_054772.1:n.1025-260_1025-259delinsAT