Canonical Allele Identifier: CA6169200

Gene: FOLR1

Linked Data

• dbSNP Id: rs760498474
• ExAC: 11:71906800 TG / T
• gnomAD v2: 11-71906800-TG-T
• MyVariant Identifiers: chr11:g.71906801del (hg19) ; chr11:g.72195757del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195760del , CM000673.2:g.72195760del	GRCh38
NC_000011.9:g.71906804del , CM000673.1:g.71906804del	GRCh37
NC_000011.8:g.71584452del	NCBI36
NG_015863.1:g.11203del

Transcript Alleles

HGVS	Amino-acid change
ENST00000312293.9:c.493+13del	ENSP00000308137.4:n.493+13del
ENST00000393676.5:c.493+13del MANE Select	ENSP00000377281.3:n.493+13del
ENST00000675784.1:c.493+13del	ENSP00000502440.1:n.493+13del
ENST00000312293.8:c.493+13del	ENSP00000308137.4:n.493+13del
ENST00000393676.3:c.493+13del	ENSP00000377281.3:n.493+13del
ENST00000393679.5:c.493+13del	ENSP00000377284.1:n.493+13del
ENST00000393681.6:c.493+13del	ENSP00000377286.2:n.493+13del
NM_000802.3:c.493+13del	NP_000793.1:n.493+13del
NM_016724.2:c.493+13del	NP_057936.1:n.493+13del
NM_016725.2:c.493+13del	NP_057937.1:n.493+13del
NM_016729.2:c.493+13del	NP_057941.1:n.493+13del
NM_016729.3:c.493+13del MANE Select	NP_057941.1:n.493+13del
NM_016724.3:c.493+13del	NP_057936.1:n.493+13del
NM_016725.3:c.493+13del	NP_057937.1:n.493+13del