Canonical Allele Identifier: CA1970377272

Gene: FOLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.49206068A= , CM000673.2:g.49206068A=	GRCh38
NC_000011.9:g.49227620A= , CM000673.1:g.49227620A=	GRCh37
NC_000011.8:g.49184196A=	NCBI36
NG_029170.1:g.7603T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256999.7:c.223T= MANE Select	ENSP00000256999.2:p.Tyr75=
ENST00000256999.6:c.223T=	ENSP00000256999.2:p.Tyr75=
ENST00000340334.11:c.178T=	ENSP00000344131.7:p.Tyr60=
ENST00000343844.8:c.-328T=	ENSP00000344086.4:n.-328T=
ENST00000356696.7:c.223T=	ENSP00000349129.3:p.Tyr75=
ENST00000525826.5:c.223T=	ENSP00000434928.1:p.Ter75=
ENST00000529117.1:c.52T=	ENSP00000431577.1:p.Tyr18=
ENST00000529646.5:n.238T=
ENST00000529648.1:c.*214T=	ENSP00000431263.1:n.*214T=
ENST00000533034.1:c.178T=	ENSP00000431463.1:p.Tyr60=
ENST00000533510.5:c.*135T=	ENSP00000436569.1:n.*135T=
NM_001014986.1:c.223T=	NP_001014986.1:p.Tyr75=
NM_001193471.1:c.178T=	NP_001180400.1:p.Tyr60=
NM_001193472.1:c.178T=	NP_001180401.1:p.Tyr60=
NM_001193473.1:c.-328T=	NP_001180402.1:n.-328T=
NM_004476.1:c.223T=	NP_004467.1:p.Tyr75=
XM_011519958.1:c.178T=	XP_011518260.1:p.Tyr60=
NM_001014986.2:c.223T=	NP_001014986.1:p.Tyr75=
NM_001193471.2:c.178T=	NP_001180400.1:p.Tyr60=
NM_001193472.2:c.178T=	NP_001180401.1:p.Tyr60=
NM_001193473.2:c.-328T=	NP_001180402.1:n.-328T=
NM_001351236.1:c.52T=	NP_001338165.1:p.Tyr18=
NM_004476.2:c.223T=	NP_004467.1:p.Tyr75=
XM_011519958.3:c.388T=	XP_011518260.2:p.Tyr130=
XM_017017432.1:c.388T=	XP_016872921.1:p.Tyr130=
XM_017017433.2:c.388T=	XP_016872922.1:p.Tyr130=
XM_017017434.1:c.178T=	XP_016872923.1:p.Tyr60=
XM_017017435.2:c.178T=	XP_016872924.1:p.Tyr60=
XM_017017444.2:c.-515T=	XP_016872933.1:n.-515T=
XM_017017445.1:c.-515T=	XP_016872934.1:n.-515T=
XM_017017446.1:c.-515T=	XP_016872935.1:n.-515T=
XM_017017447.1:c.-515T=	XP_016872936.1:n.-515T=
XM_017017448.1:c.-515T=	XP_016872937.1:n.-515T=
XM_017017449.2:c.-515T=	XP_016872938.1:n.-515T=
XM_017017450.2:c.-515T=	XP_016872939.1:n.-515T=
XM_017017451.2:c.-515T=	XP_016872940.1:n.-515T=
XM_024448411.1:c.-3916T=	XP_024304179.1:n.-3916T=
XR_001747818.1:n.618T=
XR_001747819.1:n.450T=
NM_004476.3:c.223T= MANE Select	NP_004467.1:p.Tyr75=
NM_001014986.3:c.223T=	NP_001014986.1:p.Tyr75=
NM_001193471.3:c.178T=	NP_001180400.1:p.Tyr60=
NM_001193472.3:c.178T=	NP_001180401.1:p.Tyr60=
NM_001193473.3:c.-328T=	NP_001180402.1:n.-328T=
NM_001351236.2:c.52T=	NP_001338165.1:p.Tyr18=