Canonical Allele Identifier: CA2306047287

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554105A= , CM000680.2:g.57554105A=	GRCh38
NC_000018.9:g.55221337A= , CM000680.1:g.55221337A=	GRCh37
NC_000018.8:g.53372335A=	NCBI36
NG_008175.1:g.37633T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682485.1:n.1407T=
ENST00000262093.11:c.1077+155T= MANE Select	ENSP00000262093.6:n.1077+155T=
ENST00000382873.8:c.861+155T=	ENSP00000372326.4:n.861+155T=
ENST00000651787.1:n.1183+155T=
ENST00000652755.1:c.1095+155T=	ENSP00000498358.1:n.1095+155T=
ENST00000262093.9:c.1077+155T=	ENSP00000262093.5:n.1077+155T=
ENST00000382873.7:c.1095+155T=	ENSP00000372326.3:n.1095+155T=
ENST00000585494.5:c.*804+155T=	ENSP00000465243.1:n.*804+155T=
ENST00000591977.5:c.344+155T=
NM_000140.3:c.1077+155T=	NP_000131.2:n.1077+155T=
NM_001012515.2:c.1095+155T=	NP_001012533.1:n.1095+155T=
XM_011525881.1:c.996+155T=	XP_011524183.1:n.996+155T=
XM_011525882.1:c.861+155T=	XP_011524184.1:n.861+155T=
NM_000140.4:c.1077+155T=	NP_000131.2:n.1077+155T=
NM_001012515.3:c.1095+155T=	NP_001012533.1:n.1095+155T=
XM_011525882.2:c.861+155T=	XP_011524184.1:n.861+155T=
XM_017025614.2:c.978+155T=	XP_016881103.1:n.978+155T=
NM_000140.5:c.1077+155T= MANE Select	NP_000131.2:n.1077+155T=
NM_001012515.4:c.1095+155T=	NP_001012533.1:n.1095+155T=
NM_001371094.1:c.978+155T=	NP_001358023.1:n.978+155T=
NM_001371095.1:c.861+155T=	NP_001358024.1:n.861+155T=
NM_001374778.1:c.1077+155T=	NP_001361707.1:n.1077+155T=