Canonical Allele Identifier: CA2306046202

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57551367A= , CM000680.2:g.57551367A=	GRCh38
NC_000018.9:g.55218599A= , CM000680.1:g.55218599A=	GRCh37
NC_000018.8:g.53369597A=	NCBI36
NG_008175.1:g.40371T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000140.5:c.1085T= MANE Select	NP_000131.2:p.Val362=
ENST00000262093.11:c.1085T= MANE Select	ENSP00000262093.6:p.Val362=
NM_000140.3:c.1085T=	NP_000131.2:p.Val362=
NM_000140.4:c.1085T=	NP_000131.2:p.Val362=
NM_001012515.2:c.1103T=	NP_001012533.1:p.Val368=
NM_001012515.3:c.1103T=	NP_001012533.1:p.Val368=
NM_001012515.4:c.1103T=	NP_001012533.1:p.Val368=
NM_001371094.1:c.986T=	NP_001358023.1:p.Val329=
NM_001371095.1:c.869T=	NP_001358024.1:p.Val290=
NM_001374778.1:c.1078-521T=	NP_001361707.1:n.1078-521T=
ENST00000262093.9:c.1085T=	ENSP00000262093.5:p.Val362=
ENST00000382873.7:c.1103T=	ENSP00000372326.3:p.Val368=
ENST00000382873.8:c.869T=	ENSP00000372326.4:p.Val290=
ENST00000585494.5:c.*812T=	ENSP00000465243.1:n.*812T=
ENST00000591977.5:c.352T=
ENST00000651787.1:n.1191T=
ENST00000652755.1:c.1103T=	ENSP00000498358.1:p.Val368=
XM_011525881.1:c.1004T=	XP_011524183.1:p.Val335=
XM_011525882.1:c.869T=	XP_011524184.1:p.Val290=
XM_011525882.2:c.869T=	XP_011524184.1:p.Val290=
XM_017025614.2:c.986T=	XP_016881103.1:p.Val329=