Canonical Allele Identifier: CA2306045947

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550714A= , CM000680.2:g.57550714A=	GRCh38
NC_000018.9:g.55217946A= , CM000680.1:g.55217946A=	GRCh37
NC_000018.8:g.53368944A=	NCBI36
NG_008175.1:g.41024T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1270T= MANE Select	ENSP00000262093.6:p.Ter424=
ENST00000382873.8:c.1054T=	ENSP00000372326.4:p.Ter352=
ENST00000651787.1:n.1376T=
ENST00000652755.1:c.1288T=	ENSP00000498358.1:p.Ter430=
ENST00000262093.9:c.1270T=	ENSP00000262093.5:p.Ter424=
ENST00000382873.7:c.1288T=	ENSP00000372326.3:p.Ter430=
ENST00000585494.5:c.*997T=	ENSP00000465243.1:n.*997T=
NM_000140.3:c.1270T=	NP_000131.2:p.Ter424=
NM_001012515.2:c.1288T=	NP_001012533.1:p.Ter430=
XM_011525881.1:c.1189T=	XP_011524183.1:p.Ter397=
XM_011525882.1:c.1054T=	XP_011524184.1:p.Ter352=
NM_000140.4:c.1270T=	NP_000131.2:p.Ter424=
NM_001012515.3:c.1288T=	NP_001012533.1:p.Ter430=
XM_011525882.2:c.1054T=	XP_011524184.1:p.Ter352=
XM_017025614.2:c.1171T=	XP_016881103.1:p.Ter391=
NM_000140.5:c.1270T= MANE Select	NP_000131.2:p.Ter424=
NM_001012515.4:c.1288T=	NP_001012533.1:p.Ter430=
NM_001371094.1:c.1171T=	NP_001358023.1:p.Ter391=
NM_001371095.1:c.1054T=	NP_001358024.1:p.Ter352=
NM_001374778.1:c.1210T=	NP_001361707.1:p.Ter404=