Canonical Allele Identifier: CA2306047634

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554920C= , CM000680.2:g.57554920C=	GRCh38
NC_000018.9:g.55222152C= , CM000680.1:g.55222152C=	GRCh37
NC_000018.8:g.53373150C=	NCBI36
NG_008175.1:g.36818G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.738G=	ENSP00000466263.1:p.Glu246=
ENST00000682485.1:n.1012G=
ENST00000262093.11:c.837G= MANE Select	ENSP00000262093.6:p.Glu279=
ENST00000382873.8:c.621G=	ENSP00000372326.4:p.Glu207=
ENST00000651787.1:n.943G=
ENST00000651812.1:n.434G=
ENST00000652755.1:c.855G=	ENSP00000498358.1:p.Glu285=
ENST00000262093.9:c.837G=	ENSP00000262093.5:p.Glu279=
ENST00000382873.7:c.855G=	ENSP00000372326.3:p.Glu285=
ENST00000585494.5:c.*564G=	ENSP00000465243.1:n.*564G=
ENST00000591977.5:c.104G=
ENST00000592699.5:c.738G=	ENSP00000466263.1:p.Glu246=
NM_000140.3:c.837G=	NP_000131.2:p.Glu279=
NM_001012515.2:c.855G=	NP_001012533.1:p.Glu285=
XM_011525881.1:c.756G=	XP_011524183.1:p.Glu252=
XM_011525882.1:c.621G=	XP_011524184.1:p.Glu207=
NM_000140.4:c.837G=	NP_000131.2:p.Glu279=
NM_001012515.3:c.855G=	NP_001012533.1:p.Glu285=
XM_011525882.2:c.621G=	XP_011524184.1:p.Glu207=
XM_017025614.2:c.738G=	XP_016881103.1:p.Glu246=
NM_000140.5:c.837G= MANE Select	NP_000131.2:p.Glu279=
NM_001012515.4:c.855G=	NP_001012533.1:p.Glu285=
NM_001371094.1:c.738G=	NP_001358023.1:p.Glu246=
NM_001371095.1:c.621G=	NP_001358024.1:p.Glu207=
NM_001374778.1:c.837G=	NP_001361707.1:p.Glu279=