Canonical Allele Identifier: CA2306045955

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550733G= , CM000680.2:g.57550733G=	GRCh38
NC_000018.9:g.55217965G= , CM000680.1:g.55217965G=	GRCh37
NC_000018.8:g.53368963G=	NCBI36
NG_008175.1:g.41005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1251C= MANE Select	ENSP00000262093.6:p.Phe417=
ENST00000382873.8:c.1035C=	ENSP00000372326.4:p.Phe345=
ENST00000651787.1:n.1357C=
ENST00000652755.1:c.1269C=	ENSP00000498358.1:p.Phe423=
ENST00000262093.9:c.1251C=	ENSP00000262093.5:p.Phe417=
ENST00000382873.7:c.1269C=	ENSP00000372326.3:p.Phe423=
ENST00000585494.5:c.*978C=	ENSP00000465243.1:n.*978C=
NM_000140.3:c.1251C=	NP_000131.2:p.Phe417=
NM_001012515.2:c.1269C=	NP_001012533.1:p.Phe423=
XM_011525881.1:c.1170C=	XP_011524183.1:p.Phe390=
XM_011525882.1:c.1035C=	XP_011524184.1:p.Phe345=
NM_000140.4:c.1251C=	NP_000131.2:p.Phe417=
NM_001012515.3:c.1269C=	NP_001012533.1:p.Phe423=
XM_011525882.2:c.1035C=	XP_011524184.1:p.Phe345=
XM_017025614.2:c.1152C=	XP_016881103.1:p.Phe384=
NM_000140.5:c.1251C= MANE Select	NP_000131.2:p.Phe417=
NM_001012515.4:c.1269C=	NP_001012533.1:p.Phe423=
NM_001371094.1:c.1152C=	NP_001358023.1:p.Phe384=
NM_001371095.1:c.1035C=	NP_001358024.1:p.Phe345=
NM_001374778.1:c.1191C=	NP_001361707.1:p.Phe397=