Canonical Allele Identifier: CA10646159
Gene: FLVCR2 HGNC NCBI
FLVCR2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 314404
ClinVar RCV Id: RCV000274666 RCV001786362
dbSNP Id: rs1322268460
gnomAD v2: 14-76045193-GTC-G
gnomAD v3: 14-75578850-GTC-G
gnomAD v4: 14-75578850-GTC-G
MyVariant Identifiers: chr14:g.76045197_76045198del (hg19) chr14:g.76045194_76045195del (hg19) chr14:g.75578854_75578855del (hg38) chr14:g.75578851_75578852del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75578854_75578855del , CM000676.2:g.75578854_75578855del GRCh38
NC_000014.8:g.76045197_76045198del , CM000676.1:g.76045197_76045198del GRCh37
NC_000014.7:g.75114950_75114951del NCBI36
NG_027694.1:g.5258_5259del

Transcript Alleles

HGVS Amino-acid Change
ENST00000238667.9:c.-119_-118del (FLVCR2) MANE Select ENSP00000238667.4:n.-119_-118del
ENST00000238667.8:c.-119_-118del (FLVCR2) ENSP00000238667.4:n.-119_-118del
NM_017791.2:c.-119_-118del (FLVCR2) NP_060261.2:n.-119_-118del
NR_110552.1:n.737_738del (FLVCR2-AS1)
NM_017791.3:c.-119_-118del (FLVCR2) MANE Select NP_060261.2:n.-119_-118del
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Search 100 bp 3'