Canonical Allele Identifier: CA2485643495

Gene: FLVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883650_212883651delinsCA , CM000663.2:g.212883650_212883651delinsCA	GRCh38
NC_000001.10:g.213056992_213056993delinsCA , CM000663.1:g.213056992_213056993delinsCA	GRCh37
NC_000001.9:g.211123615_211123616delinsCA	NCBI36
NG_028131.1:g.30396_30397delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+212_1092+213delinsCA MANE Select	ENSP00000355938.4:n.1092+212_1092+213delinsCA
ENST00000366971.8:c.1092+212_1092+213delinsCA	ENSP00000355938.4:n.1092+212_1092+213delinsCA
ENST00000419102.1:c.488+212_488+213delinsCA
ENST00000474693.1:n.317+212_317+213delinsCA
ENST00000483790.1:n.30+212_30+213delinsCA
NM_014053.3:c.1092+212_1092+213delinsCA	NP_054772.1:n.1092+212_1092+213delinsCA
XM_011509446.1:c.1092+212_1092+213delinsCA	XP_011507748.1:n.1092+212_1092+213delinsCA
XR_247024.1:n.1266+212_1266+213delinsCA
XR_426771.1:n.1393+212_1393+213delinsCA
XM_011509446.3:c.1092+212_1092+213delinsCA	XP_011507748.1:n.1092+212_1092+213delinsCA
XR_247024.3:n.1266+212_1266+213delinsCA
NM_014053.4:c.1092+212_1092+213delinsCA MANE Select	NP_054772.1:n.1092+212_1092+213delinsCA