Canonical Allele Identifier: CA402541176

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222109A>G (hg19) ; chr18:g.57554877A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554877A>G , CM000680.2:g.57554877A>G	GRCh38
NC_000018.9:g.55222109A>G , CM000680.1:g.55222109A>G	GRCh37
NC_000018.8:g.53373107A>G	NCBI36
NG_008175.1:g.36861T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.781T>C	ENSP00000466263.1:p.Cys261Arg
ENST00000682485.1:n.1055T>C
ENST00000262093.11:c.880T>C MANE Select	ENSP00000262093.6:p.Cys294Arg
ENST00000382873.8:c.664T>C	ENSP00000372326.4:p.Cys222Arg
ENST00000651787.1:n.986T>C
ENST00000651812.1:n.477T>C
ENST00000652755.1:c.898T>C	ENSP00000498358.1:p.Cys300Arg
ENST00000262093.9:c.880T>C	ENSP00000262093.5:p.Cys294Arg
ENST00000382873.7:c.898T>C	ENSP00000372326.3:p.Cys300Arg
ENST00000585494.5:c.*607T>C	ENSP00000465243.1:n.*607T>C
ENST00000591977.5:c.147T>C
ENST00000592699.5:c.781T>C	ENSP00000466263.1:p.Cys261Arg
NM_000140.3:c.880T>C	NP_000131.2:p.Cys294Arg
NM_001012515.2:c.898T>C	NP_001012533.1:p.Cys300Arg
XM_011525881.1:c.799T>C	XP_011524183.1:p.Cys267Arg
XM_011525882.1:c.664T>C	XP_011524184.1:p.Cys222Arg
NM_000140.4:c.880T>C	NP_000131.2:p.Cys294Arg
NM_001012515.3:c.898T>C	NP_001012533.1:p.Cys300Arg
XM_011525882.2:c.664T>C	XP_011524184.1:p.Cys222Arg
XM_017025614.2:c.781T>C	XP_016881103.1:p.Cys261Arg
NM_000140.5:c.880T>C MANE Select	NP_000131.2:p.Cys294Arg
NM_001012515.4:c.898T>C	NP_001012533.1:p.Cys300Arg
NM_001371094.1:c.781T>C	NP_001358023.1:p.Cys261Arg
NM_001371095.1:c.664T>C	NP_001358024.1:p.Cys222Arg
NM_001374778.1:c.880T>C	NP_001361707.1:p.Cys294Arg