Canonical Allele Identifier: CA2306055673

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573269G= , CM000680.2:g.57573269G=	GRCh38
NC_000018.9:g.55240501G= , CM000680.1:g.55240501G=	GRCh37
NC_000018.8:g.53391499G=	NCBI36
NG_008175.1:g.18469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.291C=	ENSP00000466263.1:p.Asp97=
ENST00000682485.1:n.403C=
ENST00000262093.11:c.291C= MANE Select	ENSP00000262093.6:p.Asp97=
ENST00000382873.8:c.75C=	ENSP00000372326.4:p.Asp25=
ENST00000651787.1:n.397C=
ENST00000652755.1:c.309C=	ENSP00000498358.1:p.Asp103=
ENST00000262093.9:c.291C=	ENSP00000262093.5:p.Asp97=
ENST00000382873.7:c.309C=	ENSP00000372326.3:p.Asp103=
ENST00000585494.5:c.291C=	ENSP00000465243.1:p.Asp97=
ENST00000585699.1:n.243C=
ENST00000585747.1:c.291C=	ENSP00000465717.1:p.Asp97=
ENST00000585878.1:n.343C=
ENST00000591215.5:c.75C=	ENSP00000467461.1:p.Asp25=
ENST00000592111.1:n.292C=
ENST00000592699.5:c.291C=	ENSP00000466263.1:p.Asp97=
NM_000140.3:c.291C=	NP_000131.2:p.Asp97=
NM_001012515.2:c.309C=	NP_001012533.1:p.Asp103=
XM_011525881.1:c.309C=	XP_011524183.1:p.Asp103=
XM_011525882.1:c.75C=	XP_011524184.1:p.Asp25=
NM_000140.4:c.291C=	NP_000131.2:p.Asp97=
NM_001012515.3:c.309C=	NP_001012533.1:p.Asp103=
XM_011525882.2:c.75C=	XP_011524184.1:p.Asp25=
XM_017025614.2:c.291C=	XP_016881103.1:p.Asp97=
NM_000140.5:c.291C= MANE Select	NP_000131.2:p.Asp97=
NM_001012515.4:c.309C=	NP_001012533.1:p.Asp103=
NM_001371094.1:c.291C=	NP_001358023.1:p.Asp97=
NM_001371095.1:c.75C=	NP_001358024.1:p.Asp25=
NM_001374778.1:c.291C=	NP_001361707.1:p.Asp97=