Canonical Allele Identifier: CA2306046186

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57551312T= , CM000680.2:g.57551312T=	GRCh38
NC_000018.9:g.55218544T= , CM000680.1:g.55218544T=	GRCh37
NC_000018.8:g.53369542T=	NCBI36
NG_008175.1:g.40426A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000140.5:c.1137+3A= MANE Select	NP_000131.2:n.1137+3A=
ENST00000262093.11:c.1137+3A= MANE Select	ENSP00000262093.6:n.1137+3A=
NM_000140.3:c.1137+3A=	NP_000131.2:n.1137+3A=
NM_000140.4:c.1137+3A=	NP_000131.2:n.1137+3A=
NM_001012515.2:c.1155+3A=	NP_001012533.1:n.1155+3A=
NM_001012515.3:c.1155+3A=	NP_001012533.1:n.1155+3A=
NM_001012515.4:c.1155+3A=	NP_001012533.1:n.1155+3A=
NM_001371094.1:c.1038+3A=	NP_001358023.1:n.1038+3A=
NM_001371095.1:c.921+3A=	NP_001358024.1:n.921+3A=
NM_001374778.1:c.1078-466A=	NP_001361707.1:n.1078-466A=
ENST00000262093.9:c.1137+3A=	ENSP00000262093.5:n.1137+3A=
ENST00000382873.7:c.1155+3A=	ENSP00000372326.3:n.1155+3A=
ENST00000382873.8:c.921+3A=	ENSP00000372326.4:n.921+3A=
ENST00000585494.5:c.*864+3A=	ENSP00000465243.1:n.*864+3A=
ENST00000591977.5:c.407A=
ENST00000651787.1:n.1243+3A=
ENST00000652755.1:c.1155+3A=	ENSP00000498358.1:n.1155+3A=
XM_011525881.1:c.1056+3A=	XP_011524183.1:n.1056+3A=
XM_011525882.1:c.921+3A=	XP_011524184.1:n.921+3A=
XM_011525882.2:c.921+3A=	XP_011524184.1:n.921+3A=
XM_017025614.2:c.1038+3A=	XP_016881103.1:n.1038+3A=