Canonical Allele Identifier: CA1970358383

Gene: FOLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.49164722G= , CM000673.2:g.49164722G=	GRCh38
NC_000011.9:g.49186274G= , CM000673.1:g.49186274G=	GRCh37
NC_000011.8:g.49142850G=	NCBI36
NG_029170.1:g.48949C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004476.3:c.1423C= MANE Select	NP_004467.1:p.His475=
ENST00000256999.7:c.1423C= MANE Select	ENSP00000256999.2:p.His475=
NM_001014986.1:c.1423C=	NP_001014986.1:p.His475=
NM_001014986.2:c.1423C=	NP_001014986.1:p.His475=
NM_001014986.3:c.1423C=	NP_001014986.1:p.His475=
NM_001193471.1:c.1378C=	NP_001180400.1:p.His460=
NM_001193471.2:c.1378C=	NP_001180400.1:p.His460=
NM_001193471.3:c.1378C=	NP_001180400.1:p.His460=
NM_001193472.1:c.1378C=	NP_001180401.1:p.His460=
NM_001193472.2:c.1378C=	NP_001180401.1:p.His460=
NM_001193472.3:c.1378C=	NP_001180401.1:p.His460=
NM_001193473.1:c.499C=	NP_001180402.1:p.His167=
NM_001193473.2:c.499C=	NP_001180402.1:p.His167=
NM_001193473.3:c.499C=	NP_001180402.1:p.His167=
NM_001351236.1:c.1252C=	NP_001338165.1:p.His418=
NM_001351236.2:c.1252C=	NP_001338165.1:p.His418=
NM_004476.1:c.1423C=	NP_004467.1:p.His475=
NM_004476.2:c.1423C=	NP_004467.1:p.His475=
ENST00000256999.6:c.1423C=	ENSP00000256999.2:p.His475=
ENST00000340334.11:c.1378C=	ENSP00000344131.7:p.His460=
ENST00000343844.8:c.499C=	ENSP00000344086.4:p.His167=
ENST00000356696.7:c.1423C=	ENSP00000349129.3:p.His475=
ENST00000458311.6:n.1025C=
ENST00000525629.1:n.506C=
ENST00000525826.5:c.*824C=	ENSP00000434928.1:n.*824C=
ENST00000533034.1:c.1378C=	ENSP00000431463.1:p.His460=
XM_011519958.1:c.1378C=	XP_011518260.1:p.His460=
XM_011519958.3:c.1588C=	XP_011518260.2:p.His530=
XM_017017432.1:c.1588C=	XP_016872921.1:p.His530=
XM_017017433.2:c.1588C=	XP_016872922.1:p.His530=
XM_017017434.1:c.1378C=	XP_016872923.1:p.His460=
XM_017017435.2:c.1378C=	XP_016872924.1:p.His460=
XM_017017444.2:c.499C=	XP_016872933.1:p.His167=
XM_017017445.1:c.499C=	XP_016872934.1:p.His167=
XM_017017446.1:c.499C=	XP_016872935.1:p.His167=
XM_017017447.1:c.499C=	XP_016872936.1:p.His167=
XM_017017448.1:c.499C=	XP_016872937.1:p.His167=
XM_017017449.2:c.499C=	XP_016872938.1:p.His167=
XM_017017450.2:c.499C=	XP_016872939.1:p.His167=
XM_017017451.2:c.499C=	XP_016872940.1:p.His167=
XM_024448411.1:c.499C=	XP_024304179.1:p.His167=
XR_001747818.1:n.1818C=
XR_001747819.1:n.1650C=