Canonical Allele Identifier: CA1012017940

Gene: FLVCR1

Linked Data

• dbSNP Id: rs1664968083
• gnomAD v3: 1-212883161-A-AG
• gnomAD v4: 1-212883161-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883161_212883162insG , CM000663.2:g.212883161_212883162insG	GRCh38
NC_000001.10:g.213056503_213056504insG , CM000663.1:g.213056503_213056504insG	GRCh37
NC_000001.9:g.211123126_211123127insG	NCBI36
NG_028131.1:g.29907_29908insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1025-210_1025-209insG MANE Select	ENSP00000355938.4:n.1025-210_1025-209insG
ENST00000366971.8:c.1025-210_1025-209insG	ENSP00000355938.4:n.1025-210_1025-209insG
ENST00000419102.1:c.421-210_421-209insG
ENST00000474693.1:n.250-210_250-209insG
NM_014053.3:c.1025-210_1025-209insG	NP_054772.1:n.1025-210_1025-209insG
XM_011509446.1:c.1025-210_1025-209insG	XP_011507748.1:n.1025-210_1025-209insG
XR_247024.1:n.1199-210_1199-209insG
XR_426771.1:n.1326-210_1326-209insG
XM_011509446.3:c.1025-210_1025-209insG	XP_011507748.1:n.1025-210_1025-209insG
XR_247024.3:n.1199-210_1199-209insG
NM_014053.4:c.1025-210_1025-209insG MANE Select	NP_054772.1:n.1025-210_1025-209insG