Canonical Allele Identifier: CA2485643342

Gene: FLVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883233_212883235delinsCTG , CM000663.2:g.212883233_212883235delinsCTG	GRCh38
NC_000001.10:g.213056575_213056577delinsCTG , CM000663.1:g.213056575_213056577delinsCTG	GRCh37
NC_000001.9:g.211123198_211123200delinsCTG	NCBI36
NG_028131.1:g.29979_29981delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1025-138_1025-136delinsCTG MANE Select	ENSP00000355938.4:n.1025-138_1025-136delinsCTG
ENST00000366971.8:c.1025-138_1025-136delinsCTG	ENSP00000355938.4:n.1025-138_1025-136delinsCTG
ENST00000419102.1:c.421-138_421-136delinsCTG
ENST00000474693.1:n.250-138_250-136delinsCTG
NM_014053.3:c.1025-138_1025-136delinsCTG	NP_054772.1:n.1025-138_1025-136delinsCTG
XM_011509446.1:c.1025-138_1025-136delinsCTG	XP_011507748.1:n.1025-138_1025-136delinsCTG
XR_247024.1:n.1199-138_1199-136delinsCTG
XR_426771.1:n.1326-138_1326-136delinsCTG
XM_011509446.3:c.1025-138_1025-136delinsCTG	XP_011507748.1:n.1025-138_1025-136delinsCTG
XR_247024.3:n.1199-138_1199-136delinsCTG
NM_014053.4:c.1025-138_1025-136delinsCTG MANE Select	NP_054772.1:n.1025-138_1025-136delinsCTG