Canonical Allele Identifier: CA2485643481

Gene: FLVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883614_212883615delinsAT , CM000663.2:g.212883614_212883615delinsAT	GRCh38
NC_000001.10:g.213056956_213056957delinsAT , CM000663.1:g.213056956_213056957delinsAT	GRCh37
NC_000001.9:g.211123579_211123580delinsAT	NCBI36
NG_028131.1:g.30360_30361delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+176_1092+177delinsAT MANE Select	ENSP00000355938.4:n.1092+176_1092+177delinsAT
ENST00000366971.8:c.1092+176_1092+177delinsAT	ENSP00000355938.4:n.1092+176_1092+177delinsAT
ENST00000419102.1:c.488+176_488+177delinsAT
ENST00000474693.1:n.317+176_317+177delinsAT
ENST00000483790.1:n.30+176_30+177delinsAT
NM_014053.3:c.1092+176_1092+177delinsAT	NP_054772.1:n.1092+176_1092+177delinsAT
XM_011509446.1:c.1092+176_1092+177delinsAT	XP_011507748.1:n.1092+176_1092+177delinsAT
XR_247024.1:n.1266+176_1266+177delinsAT
XR_426771.1:n.1393+176_1393+177delinsAT
XM_011509446.3:c.1092+176_1092+177delinsAT	XP_011507748.1:n.1092+176_1092+177delinsAT
XR_247024.3:n.1266+176_1266+177delinsAT
NM_014053.4:c.1092+176_1092+177delinsAT MANE Select	NP_054772.1:n.1092+176_1092+177delinsAT