Canonical Allele Identifier: CA2306055661

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573240T= , CM000680.2:g.57573240T=	GRCh38
NC_000018.9:g.55240472T= , CM000680.1:g.55240472T=	GRCh37
NC_000018.8:g.53391470T=	NCBI36
NG_008175.1:g.18498A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.314+6A=	ENSP00000466263.1:n.314+6A=
ENST00000682485.1:n.426+6A=
ENST00000262093.11:c.314+6A= MANE Select	ENSP00000262093.6:n.314+6A=
ENST00000382873.8:c.98+6A=	ENSP00000372326.4:n.98+6A=
ENST00000651787.1:n.420+6A=
ENST00000652755.1:c.332+6A=	ENSP00000498358.1:n.332+6A=
ENST00000262093.9:c.314+6A=	ENSP00000262093.5:n.314+6A=
ENST00000382873.7:c.332+6A=	ENSP00000372326.3:n.332+6A=
ENST00000585494.5:c.314+6A=	ENSP00000465243.1:n.314+6A=
ENST00000585699.1:n.266+6A=
ENST00000585747.1:c.314+6A=	ENSP00000465717.1:n.314+6A=
ENST00000585878.1:n.372A=
ENST00000591215.5:c.98+6A=	ENSP00000467461.1:n.98+6A=
ENST00000592111.1:n.321A=
ENST00000592699.5:c.314+6A=	ENSP00000466263.1:n.314+6A=
NM_000140.3:c.314+6A=	NP_000131.2:n.314+6A=
NM_001012515.2:c.332+6A=	NP_001012533.1:n.332+6A=
XM_011525881.1:c.332+6A=	XP_011524183.1:n.332+6A=
XM_011525882.1:c.98+6A=	XP_011524184.1:n.98+6A=
NM_000140.4:c.314+6A=	NP_000131.2:n.314+6A=
NM_001012515.3:c.332+6A=	NP_001012533.1:n.332+6A=
XM_011525882.2:c.98+6A=	XP_011524184.1:n.98+6A=
XM_017025614.2:c.314+6A=	XP_016881103.1:n.314+6A=
NM_000140.5:c.314+6A= MANE Select	NP_000131.2:n.314+6A=
NM_001012515.4:c.332+6A=	NP_001012533.1:n.332+6A=
NM_001371094.1:c.314+6A=	NP_001358023.1:n.314+6A=
NM_001371095.1:c.98+6A=	NP_001358024.1:n.98+6A=
NM_001374778.1:c.314+6A=	NP_001361707.1:n.314+6A=