Canonical Allele Identifier: CA2485643559

Gene: FLVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883807_212883808delinsTG , CM000663.2:g.212883807_212883808delinsTG	GRCh38
NC_000001.10:g.213057149_213057150delinsTG , CM000663.1:g.213057149_213057150delinsTG	GRCh37
NC_000001.9:g.211123772_211123773delinsTG	NCBI36
NG_028131.1:g.30553_30554delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+369_1092+370delinsTG MANE Select	ENSP00000355938.4:n.1092+369_1092+370delinsTG
ENST00000366971.8:c.1092+369_1092+370delinsTG	ENSP00000355938.4:n.1092+369_1092+370delinsTG
ENST00000419102.1:c.488+369_488+370delinsTG
ENST00000474693.1:n.317+369_317+370delinsTG
ENST00000483790.1:n.30+369_30+370delinsTG
NM_014053.3:c.1092+369_1092+370delinsTG	NP_054772.1:n.1092+369_1092+370delinsTG
XM_011509446.1:c.1092+369_1092+370delinsTG	XP_011507748.1:n.1092+369_1092+370delinsTG
XR_247024.1:n.1266+369_1266+370delinsTG
XR_426771.1:n.1393+369_1393+370delinsTG
XM_011509446.3:c.1092+369_1092+370delinsTG	XP_011507748.1:n.1092+369_1092+370delinsTG
XR_247024.3:n.1266+369_1266+370delinsTG
NM_014053.4:c.1092+369_1092+370delinsTG MANE Select	NP_054772.1:n.1092+369_1092+370delinsTG