Canonical Allele Identifier: CA1970377279

Gene: FOLH1

Linked Data

• dbSNP Id: rs1863898569
• gnomAD v4: 11-49206079-TTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.49206082_49206084del , CM000673.2:g.49206082_49206084del	GRCh38
NC_000011.9:g.49227634_49227636del , CM000673.1:g.49227634_49227636del	GRCh37
NC_000011.8:g.49184210_49184212del	NCBI36
NG_029170.1:g.7589_7591del

Transcript Alleles

HGVS	Amino-acid change
ENST00000256999.7:c.209_211del MANE Select	ENSP00000256999.2:p.Ile70del
ENST00000256999.6:c.209_211del	ENSP00000256999.2:p.Ile70del
ENST00000340334.11:c.164_166del	ENSP00000344131.7:p.Ile55del
ENST00000343844.8:c.-342_-340del	ENSP00000344086.4:n.-342_-340del
ENST00000356696.7:c.209_211del	ENSP00000349129.3:p.Ile70del
ENST00000525826.5:c.209_211del	ENSP00000434928.1:p.Ile70del
ENST00000529117.1:c.38_40del	ENSP00000431577.1:p.Ile13del
ENST00000529646.5:n.224_226del
ENST00000529648.1:c.*200_*202del	ENSP00000431263.1:n.*200_*202del
ENST00000533034.1:c.164_166del	ENSP00000431463.1:p.Ile55del
ENST00000533510.5:c.*121_*123del	ENSP00000436569.1:n.*121_*123del
NM_001014986.1:c.209_211del	NP_001014986.1:p.Ile70del
NM_001193471.1:c.164_166del	NP_001180400.1:p.Ile55del
NM_001193472.1:c.164_166del	NP_001180401.1:p.Ile55del
NM_001193473.1:c.-342_-340del	NP_001180402.1:n.-342_-340del
NM_004476.1:c.209_211del	NP_004467.1:p.Ile70del
XM_011519958.1:c.164_166del	XP_011518260.1:p.Ile55del
NM_001014986.2:c.209_211del	NP_001014986.1:p.Ile70del
NM_001193471.2:c.164_166del	NP_001180400.1:p.Ile55del
NM_001193472.2:c.164_166del	NP_001180401.1:p.Ile55del
NM_001193473.2:c.-342_-340del	NP_001180402.1:n.-342_-340del
NM_001351236.1:c.38_40del	NP_001338165.1:p.Ile13del
NM_004476.2:c.209_211del	NP_004467.1:p.Ile70del
XM_011519958.3:c.374_376del	XP_011518260.2:p.Ile125del
XM_017017432.1:c.374_376del	XP_016872921.1:p.Ile125del
XM_017017433.2:c.374_376del	XP_016872922.1:p.Ile125del
XM_017017434.1:c.164_166del	XP_016872923.1:p.Ile55del
XM_017017435.2:c.164_166del	XP_016872924.1:p.Ile55del
XM_017017444.2:c.-529_-527del	XP_016872933.1:n.-529_-527del
XM_017017445.1:c.-529_-527del	XP_016872934.1:n.-529_-527del
XM_017017446.1:c.-529_-527del	XP_016872935.1:n.-529_-527del
XM_017017447.1:c.-529_-527del	XP_016872936.1:n.-529_-527del
XM_017017448.1:c.-529_-527del	XP_016872937.1:n.-529_-527del
XM_017017449.2:c.-529_-527del	XP_016872938.1:n.-529_-527del
XM_017017450.2:c.-529_-527del	XP_016872939.1:n.-529_-527del
XM_017017451.2:c.-529_-527del	XP_016872940.1:n.-529_-527del
XM_024448411.1:c.-3930_-3928del	XP_024304179.1:n.-3930_-3928del
XR_001747818.1:n.604_606del
XR_001747819.1:n.436_438del
NM_004476.3:c.209_211del MANE Select	NP_004467.1:p.Ile70del
NM_001014986.3:c.209_211del	NP_001014986.1:p.Ile70del
NM_001193471.3:c.164_166del	NP_001180400.1:p.Ile55del
NM_001193472.3:c.164_166del	NP_001180401.1:p.Ile55del
NM_001193473.3:c.-342_-340del	NP_001180402.1:n.-342_-340del
NM_001351236.2:c.38_40del	NP_001338165.1:p.Ile13del