Canonical Allele Identifier: CA1970377276
Gene: FOLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.49206077T= , CM000673.2:g.49206077T= GRCh38
NC_000011.9:g.49227629T= , CM000673.1:g.49227629T= GRCh37
NC_000011.8:g.49184205T= NCBI36
NG_029170.1:g.7594A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256999.7:c.214A= MANE Select ENSP00000256999.2:p.Lys72=
ENST00000256999.6:c.214A= ENSP00000256999.2:p.Lys72=
ENST00000340334.11:c.169A= ENSP00000344131.7:p.Lys57=
ENST00000343844.8:c.-337A= ENSP00000344086.4:n.-337A=
ENST00000356696.7:c.214A= ENSP00000349129.3:p.Lys72=
ENST00000525826.5:c.214A= ENSP00000434928.1:p.Lys72=
ENST00000529117.1:c.43A= ENSP00000431577.1:p.Lys15=
ENST00000529646.5:n.229A=
ENST00000529648.1:c.*205A= ENSP00000431263.1:n.*205A=
ENST00000533034.1:c.169A= ENSP00000431463.1:p.Lys57=
ENST00000533510.5:c.*126A= ENSP00000436569.1:n.*126A=
NM_001014986.1:c.214A= NP_001014986.1:p.Lys72=
NM_001193471.1:c.169A= NP_001180400.1:p.Lys57=
NM_001193472.1:c.169A= NP_001180401.1:p.Lys57=
NM_001193473.1:c.-337A= NP_001180402.1:n.-337A=
NM_004476.1:c.214A= NP_004467.1:p.Lys72=
XM_011519958.1:c.169A= XP_011518260.1:p.Lys57=
NM_001014986.2:c.214A= NP_001014986.1:p.Lys72=
NM_001193471.2:c.169A= NP_001180400.1:p.Lys57=
NM_001193472.2:c.169A= NP_001180401.1:p.Lys57=
NM_001193473.2:c.-337A= NP_001180402.1:n.-337A=
NM_001351236.1:c.43A= NP_001338165.1:p.Lys15=
NM_004476.2:c.214A= NP_004467.1:p.Lys72=
XM_011519958.3:c.379A= XP_011518260.2:p.Lys127=
XM_017017432.1:c.379A= XP_016872921.1:p.Lys127=
XM_017017433.2:c.379A= XP_016872922.1:p.Lys127=
XM_017017434.1:c.169A= XP_016872923.1:p.Lys57=
XM_017017435.2:c.169A= XP_016872924.1:p.Lys57=
XM_017017444.2:c.-524A= XP_016872933.1:n.-524A=
XM_017017445.1:c.-524A= XP_016872934.1:n.-524A=
XM_017017446.1:c.-524A= XP_016872935.1:n.-524A=
XM_017017447.1:c.-524A= XP_016872936.1:n.-524A=
XM_017017448.1:c.-524A= XP_016872937.1:n.-524A=
XM_017017449.2:c.-524A= XP_016872938.1:n.-524A=
XM_017017450.2:c.-524A= XP_016872939.1:n.-524A=
XM_017017451.2:c.-524A= XP_016872940.1:n.-524A=
XM_024448411.1:c.-3925A= XP_024304179.1:n.-3925A=
XR_001747818.1:n.609A=
XR_001747819.1:n.441A=
NM_004476.3:c.214A= MANE Select NP_004467.1:p.Lys72=
NM_001014986.3:c.214A= NP_001014986.1:p.Lys72=
NM_001193471.3:c.169A= NP_001180400.1:p.Lys57=
NM_001193472.3:c.169A= NP_001180401.1:p.Lys57=
NM_001193473.3:c.-337A= NP_001180402.1:n.-337A=
NM_001351236.2:c.43A= NP_001338165.1:p.Lys15=