Canonical Allele Identifier: CA2306055630

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573169G= , CM000680.2:g.57573169G=	GRCh38
NC_000018.9:g.55240401G= , CM000680.1:g.55240401G=	GRCh37
NC_000018.8:g.53391399G=	NCBI36
NG_008175.1:g.18569C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.314+77C=	ENSP00000466263.1:n.314+77C=
ENST00000682485.1:n.426+77C=
ENST00000262093.11:c.314+77C= MANE Select	ENSP00000262093.6:n.314+77C=
ENST00000382873.8:c.98+77C=	ENSP00000372326.4:n.98+77C=
ENST00000651787.1:n.420+77C=
ENST00000652755.1:c.332+77C=	ENSP00000498358.1:n.332+77C=
ENST00000262093.9:c.314+77C=	ENSP00000262093.5:n.314+77C=
ENST00000382873.7:c.332+77C=	ENSP00000372326.3:n.332+77C=
ENST00000585494.5:c.314+77C=	ENSP00000465243.1:n.314+77C=
ENST00000585699.1:n.266+77C=
ENST00000585747.1:c.314+77C=	ENSP00000465717.1:n.314+77C=
ENST00000585878.1:n.443C=
ENST00000591215.5:c.98+77C=	ENSP00000467461.1:n.98+77C=
ENST00000592111.1:n.392C=
ENST00000592699.5:c.314+77C=	ENSP00000466263.1:n.314+77C=
NM_000140.3:c.314+77C=	NP_000131.2:n.314+77C=
NM_001012515.2:c.332+77C=	NP_001012533.1:n.332+77C=
XM_011525881.1:c.332+77C=	XP_011524183.1:n.332+77C=
XM_011525882.1:c.98+77C=	XP_011524184.1:n.98+77C=
NM_000140.4:c.314+77C=	NP_000131.2:n.314+77C=
NM_001012515.3:c.332+77C=	NP_001012533.1:n.332+77C=
XM_011525882.2:c.98+77C=	XP_011524184.1:n.98+77C=
XM_017025614.2:c.314+77C=	XP_016881103.1:n.314+77C=
NM_000140.5:c.314+77C= MANE Select	NP_000131.2:n.314+77C=
NM_001012515.4:c.332+77C=	NP_001012533.1:n.332+77C=
NM_001371094.1:c.314+77C=	NP_001358023.1:n.314+77C=
NM_001371095.1:c.98+77C=	NP_001358024.1:n.98+77C=
NM_001374778.1:c.314+77C=	NP_001361707.1:n.314+77C=