Canonical Allele Identifier: CA224399058

Gene: FOLR1

Linked Data

• dbSNP Id: rs556423818
• gnomAD v2: 11-71901031-TGAGTTCTCAGCTCTTCTAGTCTGGG-T
• gnomAD v3: 11-72189987-TGAGTTCTCAGCTCTTCTAGTCTGGG-T
• gnomAD v4: 11-72189987-TGAGTTCTCAGCTCTTCTAGTCTGGG-T
• MyVariant Identifiers: chr11:g.71901032_71901056del (hg19) ; chr11:g.72189988_72190012del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72189989_72190013del , CM000673.2:g.72189989_72190013del	GRCh38
NC_000011.9:g.71901033_71901057del , CM000673.1:g.71901033_71901057del	GRCh37
NC_000011.8:g.71578681_71578705del	NCBI36
NG_015863.1:g.5432_5456del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.-9+230_-9+254del	ENSP00000308137.4:n.-9+230_-9+254del
ENST00000675784.1:c.-9+58_-9+82del	ENSP00000502440.1:n.-9+58_-9+82del
ENST00000312293.8:c.-9+230_-9+254del	ENSP00000308137.4:n.-9+230_-9+254del
ENST00000393681.6:c.-75+230_-75+254del	ENSP00000377286.2:n.-75+230_-75+254del
NM_000802.3:c.-9+58_-9+82del	NP_000793.1:n.-9+58_-9+82del
NM_016724.2:c.-75+230_-75+254del	NP_057936.1:n.-75+230_-75+254del
NM_016725.2:c.-9+230_-9+254del	NP_057937.1:n.-9+230_-9+254del
NM_016724.3:c.-75+230_-75+254del	NP_057936.1:n.-75+230_-75+254del
NM_016725.3:c.-9+230_-9+254del	NP_057937.1:n.-9+230_-9+254del