Canonical Allele Identifier: CA2306047621

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554871G= , CM000680.2:g.57554871G=	GRCh38
NC_000018.9:g.55222103G= , CM000680.1:g.55222103G=	GRCh37
NC_000018.8:g.53373101G=	NCBI36
NG_008175.1:g.36867C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.787C=	ENSP00000466263.1:p.Pro263=
ENST00000682485.1:n.1061C=
ENST00000262093.11:c.886C= MANE Select	ENSP00000262093.6:p.Pro296=
ENST00000382873.8:c.670C=	ENSP00000372326.4:p.Pro224=
ENST00000651787.1:n.992C=
ENST00000651812.1:n.483C=
ENST00000652755.1:c.904C=	ENSP00000498358.1:p.Pro302=
ENST00000262093.9:c.886C=	ENSP00000262093.5:p.Pro296=
ENST00000382873.7:c.904C=	ENSP00000372326.3:p.Pro302=
ENST00000585494.5:c.*613C=	ENSP00000465243.1:n.*613C=
ENST00000591977.5:c.153C=
ENST00000592699.5:c.787C=	ENSP00000466263.1:p.Pro263=
NM_000140.3:c.886C=	NP_000131.2:p.Pro296=
NM_001012515.2:c.904C=	NP_001012533.1:p.Pro302=
XM_011525881.1:c.805C=	XP_011524183.1:p.Pro269=
XM_011525882.1:c.670C=	XP_011524184.1:p.Pro224=
NM_000140.4:c.886C=	NP_000131.2:p.Pro296=
NM_001012515.3:c.904C=	NP_001012533.1:p.Pro302=
XM_011525882.2:c.670C=	XP_011524184.1:p.Pro224=
XM_017025614.2:c.787C=	XP_016881103.1:p.Pro263=
NM_000140.5:c.886C= MANE Select	NP_000131.2:p.Pro296=
NM_001012515.4:c.904C=	NP_001012533.1:p.Pro302=
NM_001371094.1:c.787C=	NP_001358023.1:p.Pro263=
NM_001371095.1:c.670C=	NP_001358024.1:p.Pro224=
NM_001374778.1:c.886C=	NP_001361707.1:p.Pro296=