Canonical Allele Identifier: CA2306047550

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554726A= , CM000680.2:g.57554726A=	GRCh38
NC_000018.9:g.55221958A= , CM000680.1:g.55221958A=	GRCh37
NC_000018.8:g.53372956A=	NCBI36
NG_008175.1:g.37012T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.813+119T=	ENSP00000466263.1:n.813+119T=
ENST00000682485.1:n.1087+119T=
ENST00000262093.11:c.912+119T= MANE Select	ENSP00000262093.6:n.912+119T=
ENST00000382873.8:c.696+119T=	ENSP00000372326.4:n.696+119T=
ENST00000651787.1:n.1018+119T=
ENST00000651812.1:n.509+119T=
ENST00000652755.1:c.930+119T=	ENSP00000498358.1:n.930+119T=
ENST00000262093.9:c.912+119T=	ENSP00000262093.5:n.912+119T=
ENST00000382873.7:c.930+119T=	ENSP00000372326.3:n.930+119T=
ENST00000585494.5:c.*639+119T=	ENSP00000465243.1:n.*639+119T=
ENST00000591977.5:c.179+119T=
ENST00000592699.5:c.813+119T=	ENSP00000466263.1:n.813+119T=
NM_000140.3:c.912+119T=	NP_000131.2:n.912+119T=
NM_001012515.2:c.930+119T=	NP_001012533.1:n.930+119T=
XM_011525881.1:c.831+119T=	XP_011524183.1:n.831+119T=
XM_011525882.1:c.696+119T=	XP_011524184.1:n.696+119T=
NM_000140.4:c.912+119T=	NP_000131.2:n.912+119T=
NM_001012515.3:c.930+119T=	NP_001012533.1:n.930+119T=
XM_011525882.2:c.696+119T=	XP_011524184.1:n.696+119T=
XM_017025614.2:c.813+119T=	XP_016881103.1:n.813+119T=
NM_000140.5:c.912+119T= MANE Select	NP_000131.2:n.912+119T=
NM_001012515.4:c.930+119T=	NP_001012533.1:n.930+119T=
NM_001371094.1:c.813+119T=	NP_001358023.1:n.813+119T=
NM_001371095.1:c.696+119T=	NP_001358024.1:n.696+119T=
NM_001374778.1:c.912+119T=	NP_001361707.1:n.912+119T=