Canonical Allele Identifier: CA2306047645

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554952C= , CM000680.2:g.57554952C=	GRCh38
NC_000018.9:g.55222184C= , CM000680.1:g.55222184C=	GRCh37
NC_000018.8:g.53373182C=	NCBI36
NG_008175.1:g.36786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.706G=	ENSP00000466263.1:p.Val236=
ENST00000682485.1:n.980G=
ENST00000262093.11:c.805G= MANE Select	ENSP00000262093.6:p.Val269=
ENST00000382873.8:c.589G=	ENSP00000372326.4:p.Val197=
ENST00000651787.1:n.911G=
ENST00000651812.1:n.402G=
ENST00000652755.1:c.823G=	ENSP00000498358.1:p.Val275=
ENST00000262093.9:c.805G=	ENSP00000262093.5:p.Val269=
ENST00000382873.7:c.823G=	ENSP00000372326.3:p.Val275=
ENST00000585494.5:c.*532G=	ENSP00000465243.1:n.*532G=
ENST00000591977.5:c.72G=
ENST00000592699.5:c.706G=	ENSP00000466263.1:p.Val236=
NM_000140.3:c.805G=	NP_000131.2:p.Val269=
NM_001012515.2:c.823G=	NP_001012533.1:p.Val275=
XM_011525881.1:c.724G=	XP_011524183.1:p.Val242=
XM_011525882.1:c.589G=	XP_011524184.1:p.Val197=
NM_000140.4:c.805G=	NP_000131.2:p.Val269=
NM_001012515.3:c.823G=	NP_001012533.1:p.Val275=
XM_011525882.2:c.589G=	XP_011524184.1:p.Val197=
XM_017025614.2:c.706G=	XP_016881103.1:p.Val236=
NM_000140.5:c.805G= MANE Select	NP_000131.2:p.Val269=
NM_001012515.4:c.823G=	NP_001012533.1:p.Val275=
NM_001371094.1:c.706G=	NP_001358023.1:p.Val236=
NM_001371095.1:c.589G=	NP_001358024.1:p.Val197=
NM_001374778.1:c.805G=	NP_001361707.1:p.Val269=