Canonical Allele Identifier: CA380439521

Gene: FOLH1

Linked Data

• MyVariant Identifiers: chr11:g.49227623A>C (hg19) ; chr11:g.49206071A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.49206071A>C , CM000673.2:g.49206071A>C	GRCh38
NC_000011.9:g.49227623A>C , CM000673.1:g.49227623A>C	GRCh37
NC_000011.8:g.49184199A>C	NCBI36
NG_029170.1:g.7600T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000256999.7:c.220T>G MANE Select	ENSP00000256999.2:p.Leu74Val
ENST00000256999.6:c.220T>G	ENSP00000256999.2:p.Leu74Val
ENST00000340334.11:c.175T>G	ENSP00000344131.7:p.Leu59Val
ENST00000343844.8:c.-331T>G	ENSP00000344086.4:n.-331T>G
ENST00000356696.7:c.220T>G	ENSP00000349129.3:p.Leu74Val
ENST00000525826.5:c.220T>G	ENSP00000434928.1:p.Leu74Val
ENST00000529117.1:c.49T>G	ENSP00000431577.1:p.Leu17Val
ENST00000529646.5:n.235T>G
ENST00000529648.1:c.*211T>G	ENSP00000431263.1:n.*211T>G
ENST00000533034.1:c.175T>G	ENSP00000431463.1:p.Leu59Val
ENST00000533510.5:c.*132T>G	ENSP00000436569.1:n.*132T>G
NM_001014986.1:c.220T>G	NP_001014986.1:p.Leu74Val
NM_001193471.1:c.175T>G	NP_001180400.1:p.Leu59Val
NM_001193472.1:c.175T>G	NP_001180401.1:p.Leu59Val
NM_001193473.1:c.-331T>G	NP_001180402.1:n.-331T>G
NM_004476.1:c.220T>G	NP_004467.1:p.Leu74Val
XM_011519958.1:c.175T>G	XP_011518260.1:p.Leu59Val
NM_001014986.2:c.220T>G	NP_001014986.1:p.Leu74Val
NM_001193471.2:c.175T>G	NP_001180400.1:p.Leu59Val
NM_001193472.2:c.175T>G	NP_001180401.1:p.Leu59Val
NM_001193473.2:c.-331T>G	NP_001180402.1:n.-331T>G
NM_001351236.1:c.49T>G	NP_001338165.1:p.Leu17Val
NM_004476.2:c.220T>G	NP_004467.1:p.Leu74Val
XM_011519958.3:c.385T>G	XP_011518260.2:p.Leu129Val
XM_017017432.1:c.385T>G	XP_016872921.1:p.Leu129Val
XM_017017433.2:c.385T>G	XP_016872922.1:p.Leu129Val
XM_017017434.1:c.175T>G	XP_016872923.1:p.Leu59Val
XM_017017435.2:c.175T>G	XP_016872924.1:p.Leu59Val
XM_017017444.2:c.-518T>G	XP_016872933.1:n.-518T>G
XM_017017445.1:c.-518T>G	XP_016872934.1:n.-518T>G
XM_017017446.1:c.-518T>G	XP_016872935.1:n.-518T>G
XM_017017447.1:c.-518T>G	XP_016872936.1:n.-518T>G
XM_017017448.1:c.-518T>G	XP_016872937.1:n.-518T>G
XM_017017449.2:c.-518T>G	XP_016872938.1:n.-518T>G
XM_017017450.2:c.-518T>G	XP_016872939.1:n.-518T>G
XM_017017451.2:c.-518T>G	XP_016872940.1:n.-518T>G
XM_024448411.1:c.-3919T>G	XP_024304179.1:n.-3919T>G
XR_001747818.1:n.615T>G
XR_001747819.1:n.447T>G
NM_004476.3:c.220T>G MANE Select	NP_004467.1:p.Leu74Val
NM_001014986.3:c.220T>G	NP_001014986.1:p.Leu74Val
NM_001193471.3:c.175T>G	NP_001180400.1:p.Leu59Val
NM_001193472.3:c.175T>G	NP_001180401.1:p.Leu59Val
NM_001193473.3:c.-331T>G	NP_001180402.1:n.-331T>G
NM_001351236.2:c.49T>G	NP_001338165.1:p.Leu17Val