Canonical Allele Identifier: CA402541105

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222090A>T (hg19) ; chr18:g.57554858A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554858A>T , CM000680.2:g.57554858A>T	GRCh38
NC_000018.9:g.55222090A>T , CM000680.1:g.55222090A>T	GRCh37
NC_000018.8:g.53373088A>T	NCBI36
NG_008175.1:g.36880T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.800T>A	ENSP00000466263.1:p.Val267Glu
ENST00000682485.1:n.1074T>A
ENST00000262093.11:c.899T>A MANE Select	ENSP00000262093.6:p.Val300Glu
ENST00000382873.8:c.683T>A	ENSP00000372326.4:p.Val228Glu
ENST00000651787.1:n.1005T>A
ENST00000651812.1:n.496T>A
ENST00000652755.1:c.917T>A	ENSP00000498358.1:p.Val306Glu
ENST00000262093.9:c.899T>A	ENSP00000262093.5:p.Val300Glu
ENST00000382873.7:c.917T>A	ENSP00000372326.3:p.Val306Glu
ENST00000585494.5:c.*626T>A	ENSP00000465243.1:n.*626T>A
ENST00000591977.5:c.166T>A
ENST00000592699.5:c.800T>A	ENSP00000466263.1:p.Val267Glu
NM_000140.3:c.899T>A	NP_000131.2:p.Val300Glu
NM_001012515.2:c.917T>A	NP_001012533.1:p.Val306Glu
XM_011525881.1:c.818T>A	XP_011524183.1:p.Val273Glu
XM_011525882.1:c.683T>A	XP_011524184.1:p.Val228Glu
NM_000140.4:c.899T>A	NP_000131.2:p.Val300Glu
NM_001012515.3:c.917T>A	NP_001012533.1:p.Val306Glu
XM_011525882.2:c.683T>A	XP_011524184.1:p.Val228Glu
XM_017025614.2:c.800T>A	XP_016881103.1:p.Val267Glu
NM_000140.5:c.899T>A MANE Select	NP_000131.2:p.Val300Glu
NM_001012515.4:c.917T>A	NP_001012533.1:p.Val306Glu
NM_001371094.1:c.800T>A	NP_001358023.1:p.Val267Glu
NM_001371095.1:c.683T>A	NP_001358024.1:p.Val228Glu
NM_001374778.1:c.899T>A	NP_001361707.1:p.Val300Glu