Canonical Allele Identifier: CA2485643415

Gene: FLVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883443_212883446delinsGCTT , CM000663.2:g.212883443_212883446delinsGCTT	GRCh38
NC_000001.10:g.213056785_213056788delinsGCTT , CM000663.1:g.213056785_213056788delinsGCTT	GRCh37
NC_000001.9:g.211123408_211123411delinsGCTT	NCBI36
NG_028131.1:g.30189_30192delinsGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+5_1092+8delinsGCTT MANE Select	ENSP00000355938.4:n.1092+5_1092+8delinsGCTT
ENST00000366971.8:c.1092+5_1092+8delinsGCTT	ENSP00000355938.4:n.1092+5_1092+8delinsGCTT
ENST00000419102.1:c.488+5_488+8delinsGCTT
ENST00000474693.1:n.317+5_317+8delinsGCTT
ENST00000483790.1:n.30+5_30+8delinsGCTT
NM_014053.3:c.1092+5_1092+8delinsGCTT	NP_054772.1:n.1092+5_1092+8delinsGCTT
XM_011509446.1:c.1092+5_1092+8delinsGCTT	XP_011507748.1:n.1092+5_1092+8delinsGCTT
XR_247024.1:n.1266+5_1266+8delinsGCTT
XR_426771.1:n.1393+5_1393+8delinsGCTT
XM_011509446.3:c.1092+5_1092+8delinsGCTT	XP_011507748.1:n.1092+5_1092+8delinsGCTT
XR_247024.3:n.1266+5_1266+8delinsGCTT
NM_014053.4:c.1092+5_1092+8delinsGCTT MANE Select	NP_054772.1:n.1092+5_1092+8delinsGCTT