Canonical Allele Identifier: CA474277475

Gene: FOLH1

Linked Data

• MyVariant Identifiers: chr11:g.49227624G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.49206072G>A , CM000673.2:g.49206072G>A	GRCh38
NC_000011.9:g.49227624G>A , CM000673.1:g.49227624G>A	GRCh37
NC_000011.8:g.49184200G>A	NCBI36
NG_029170.1:g.7599C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000256999.7:c.219C>T MANE Select	ENSP00000256999.2:p.Phe73=
ENST00000256999.6:c.219C>T	ENSP00000256999.2:p.Phe73=
ENST00000340334.11:c.174C>T	ENSP00000344131.7:p.Phe58=
ENST00000343844.8:c.-332C>T	ENSP00000344086.4:n.-332C>T
ENST00000356696.7:c.219C>T	ENSP00000349129.3:p.Phe73=
ENST00000525826.5:c.219C>T	ENSP00000434928.1:p.Phe73=
ENST00000529117.1:c.48C>T	ENSP00000431577.1:p.Phe16=
ENST00000529646.5:n.234C>T
ENST00000529648.1:c.*210C>T	ENSP00000431263.1:n.*210C>T
ENST00000533034.1:c.174C>T	ENSP00000431463.1:p.Phe58=
ENST00000533510.5:c.*131C>T	ENSP00000436569.1:n.*131C>T
NM_001014986.1:c.219C>T	NP_001014986.1:p.Phe73=
NM_001193471.1:c.174C>T	NP_001180400.1:p.Phe58=
NM_001193472.1:c.174C>T	NP_001180401.1:p.Phe58=
NM_001193473.1:c.-332C>T	NP_001180402.1:n.-332C>T
NM_004476.1:c.219C>T	NP_004467.1:p.Phe73=
XM_011519958.1:c.174C>T	XP_011518260.1:p.Phe58=
NM_001014986.2:c.219C>T	NP_001014986.1:p.Phe73=
NM_001193471.2:c.174C>T	NP_001180400.1:p.Phe58=
NM_001193472.2:c.174C>T	NP_001180401.1:p.Phe58=
NM_001193473.2:c.-332C>T	NP_001180402.1:n.-332C>T
NM_001351236.1:c.48C>T	NP_001338165.1:p.Phe16=
NM_004476.2:c.219C>T	NP_004467.1:p.Phe73=
XM_011519958.3:c.384C>T	XP_011518260.2:p.Phe128=
XM_017017432.1:c.384C>T	XP_016872921.1:p.Phe128=
XM_017017433.2:c.384C>T	XP_016872922.1:p.Phe128=
XM_017017434.1:c.174C>T	XP_016872923.1:p.Phe58=
XM_017017435.2:c.174C>T	XP_016872924.1:p.Phe58=
XM_017017444.2:c.-519C>T	XP_016872933.1:n.-519C>T
XM_017017445.1:c.-519C>T	XP_016872934.1:n.-519C>T
XM_017017446.1:c.-519C>T	XP_016872935.1:n.-519C>T
XM_017017447.1:c.-519C>T	XP_016872936.1:n.-519C>T
XM_017017448.1:c.-519C>T	XP_016872937.1:n.-519C>T
XM_017017449.2:c.-519C>T	XP_016872938.1:n.-519C>T
XM_017017450.2:c.-519C>T	XP_016872939.1:n.-519C>T
XM_017017451.2:c.-519C>T	XP_016872940.1:n.-519C>T
XM_024448411.1:c.-3920C>T	XP_024304179.1:n.-3920C>T
XR_001747818.1:n.614C>T
XR_001747819.1:n.446C>T
NM_004476.3:c.219C>T MANE Select	NP_004467.1:p.Phe73=
NM_001014986.3:c.219C>T	NP_001014986.1:p.Phe73=
NM_001193471.3:c.174C>T	NP_001180400.1:p.Phe58=
NM_001193472.3:c.174C>T	NP_001180401.1:p.Phe58=
NM_001193473.3:c.-332C>T	NP_001180402.1:n.-332C>T
NM_001351236.2:c.48C>T	NP_001338165.1:p.Phe16=