Canonical Allele Identifier: CA2306047632

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554913C= , CM000680.2:g.57554913C=	GRCh38
NC_000018.9:g.55222145C= , CM000680.1:g.55222145C=	GRCh37
NC_000018.8:g.53373143C=	NCBI36
NG_008175.1:g.36825G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.745G=	ENSP00000466263.1:p.Ala249=
ENST00000682485.1:n.1019G=
ENST00000262093.11:c.844G= MANE Select	ENSP00000262093.6:p.Ala282=
ENST00000382873.8:c.628G=	ENSP00000372326.4:p.Ala210=
ENST00000651787.1:n.950G=
ENST00000651812.1:n.441G=
ENST00000652755.1:c.862G=	ENSP00000498358.1:p.Ala288=
ENST00000262093.9:c.844G=	ENSP00000262093.5:p.Ala282=
ENST00000382873.7:c.862G=	ENSP00000372326.3:p.Ala288=
ENST00000585494.5:c.*571G=	ENSP00000465243.1:n.*571G=
ENST00000591977.5:c.111G=
ENST00000592699.5:c.745G=	ENSP00000466263.1:p.Ala249=
NM_000140.3:c.844G=	NP_000131.2:p.Ala282=
NM_001012515.2:c.862G=	NP_001012533.1:p.Ala288=
XM_011525881.1:c.763G=	XP_011524183.1:p.Ala255=
XM_011525882.1:c.628G=	XP_011524184.1:p.Ala210=
NM_000140.4:c.844G=	NP_000131.2:p.Ala282=
NM_001012515.3:c.862G=	NP_001012533.1:p.Ala288=
XM_011525882.2:c.628G=	XP_011524184.1:p.Ala210=
XM_017025614.2:c.745G=	XP_016881103.1:p.Ala249=
NM_000140.5:c.844G= MANE Select	NP_000131.2:p.Ala282=
NM_001012515.4:c.862G=	NP_001012533.1:p.Ala288=
NM_001371094.1:c.745G=	NP_001358023.1:p.Ala249=
NM_001371095.1:c.628G=	NP_001358024.1:p.Ala210=
NM_001374778.1:c.844G=	NP_001361707.1:p.Ala282=