Canonical Allele Identifier: CA2306047263

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554065C= , CM000680.2:g.57554065C=	GRCh38
NC_000018.9:g.55221297C= , CM000680.1:g.55221297C=	GRCh37
NC_000018.8:g.53372295C=	NCBI36
NG_008175.1:g.37673G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682485.1:n.1447G=
ENST00000262093.11:c.1077+195G= MANE Select	ENSP00000262093.6:n.1077+195G=
ENST00000382873.8:c.861+195G=	ENSP00000372326.4:n.861+195G=
ENST00000651787.1:n.1183+195G=
ENST00000652755.1:c.1095+195G=	ENSP00000498358.1:n.1095+195G=
ENST00000262093.9:c.1077+195G=	ENSP00000262093.5:n.1077+195G=
ENST00000382873.7:c.1095+195G=	ENSP00000372326.3:n.1095+195G=
ENST00000585494.5:c.*804+195G=	ENSP00000465243.1:n.*804+195G=
ENST00000591977.5:c.344+195G=
NM_000140.3:c.1077+195G=	NP_000131.2:n.1077+195G=
NM_001012515.2:c.1095+195G=	NP_001012533.1:n.1095+195G=
XM_011525881.1:c.996+195G=	XP_011524183.1:n.996+195G=
XM_011525882.1:c.861+195G=	XP_011524184.1:n.861+195G=
NM_000140.4:c.1077+195G=	NP_000131.2:n.1077+195G=
NM_001012515.3:c.1095+195G=	NP_001012533.1:n.1095+195G=
XM_011525882.2:c.861+195G=	XP_011524184.1:n.861+195G=
XM_017025614.2:c.978+195G=	XP_016881103.1:n.978+195G=
NM_000140.5:c.1077+195G= MANE Select	NP_000131.2:n.1077+195G=
NM_001012515.4:c.1095+195G=	NP_001012533.1:n.1095+195G=
NM_001371094.1:c.978+195G=	NP_001358023.1:n.978+195G=
NM_001371095.1:c.861+195G=	NP_001358024.1:n.861+195G=
NM_001374778.1:c.1077+195G=	NP_001361707.1:n.1077+195G=