Canonical Allele Identifier: CA2306045888

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550615T= , CM000680.2:g.57550615T=	GRCh38
NC_000018.9:g.55217847T= , CM000680.1:g.55217847T=	GRCh37
NC_000018.8:g.53368845T=	NCBI36
NG_008175.1:g.41123A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262093.11:c.*97A= MANE Select	ENSP00000262093.6:n.*97A=
ENST00000382873.8:c.*97A=	ENSP00000372326.4:n.*97A=
ENST00000651787.1:n.1475A=
ENST00000652755.1:c.*97A=	ENSP00000498358.1:n.*97A=
ENST00000262093.9:c.*97A=	ENSP00000262093.5:n.*97A=
ENST00000382873.7:c.*97A=	ENSP00000372326.3:n.*97A=
ENST00000585494.5:c.*1096A=	ENSP00000465243.1:n.*1096A=
NM_000140.3:c.*97A=	NP_000131.2:n.*97A=
NM_001012515.2:c.*97A=	NP_001012533.1:n.*97A=
XM_011525881.1:c.*97A=	XP_011524183.1:n.*97A=
XM_011525882.1:c.*97A=	XP_011524184.1:n.*97A=
NM_000140.4:c.*97A=	NP_000131.2:n.*97A=
NM_001012515.3:c.*97A=	NP_001012533.1:n.*97A=
XM_011525882.2:c.*97A=	XP_011524184.1:n.*97A=
XM_017025614.2:c.*97A=	XP_016881103.1:n.*97A=
NM_000140.5:c.*97A= MANE Select	NP_000131.2:n.*97A=
NM_001012515.4:c.*97A=	NP_001012533.1:n.*97A=
NM_001371094.1:c.*97A=	NP_001358023.1:n.*97A=
NM_001371095.1:c.*97A=	NP_001358024.1:n.*97A=
NM_001374778.1:c.*97A=	NP_001361707.1:n.*97A=