Canonical Allele Identifier: CA402541163

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222107G>C (hg19) ; chr18:g.57554875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554875G>C , CM000680.2:g.57554875G>C	GRCh38
NC_000018.9:g.55222107G>C , CM000680.1:g.55222107G>C	GRCh37
NC_000018.8:g.53373105G>C	NCBI36
NG_008175.1:g.36863C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.783C>G	ENSP00000466263.1:p.Cys261Trp
ENST00000682485.1:n.1057C>G
ENST00000262093.11:c.882C>G MANE Select	ENSP00000262093.6:p.Cys294Trp
ENST00000382873.8:c.666C>G	ENSP00000372326.4:p.Cys222Trp
ENST00000651787.1:n.988C>G
ENST00000651812.1:n.479C>G
ENST00000652755.1:c.900C>G	ENSP00000498358.1:p.Cys300Trp
ENST00000262093.9:c.882C>G	ENSP00000262093.5:p.Cys294Trp
ENST00000382873.7:c.900C>G	ENSP00000372326.3:p.Cys300Trp
ENST00000585494.5:c.*609C>G	ENSP00000465243.1:n.*609C>G
ENST00000591977.5:c.149C>G
ENST00000592699.5:c.783C>G	ENSP00000466263.1:p.Cys261Trp
NM_000140.3:c.882C>G	NP_000131.2:p.Cys294Trp
NM_001012515.2:c.900C>G	NP_001012533.1:p.Cys300Trp
XM_011525881.1:c.801C>G	XP_011524183.1:p.Cys267Trp
XM_011525882.1:c.666C>G	XP_011524184.1:p.Cys222Trp
NM_000140.4:c.882C>G	NP_000131.2:p.Cys294Trp
NM_001012515.3:c.900C>G	NP_001012533.1:p.Cys300Trp
XM_011525882.2:c.666C>G	XP_011524184.1:p.Cys222Trp
XM_017025614.2:c.783C>G	XP_016881103.1:p.Cys261Trp
NM_000140.5:c.882C>G MANE Select	NP_000131.2:p.Cys294Trp
NM_001012515.4:c.900C>G	NP_001012533.1:p.Cys300Trp
NM_001371094.1:c.783C>G	NP_001358023.1:p.Cys261Trp
NM_001371095.1:c.666C>G	NP_001358024.1:p.Cys222Trp
NM_001374778.1:c.882C>G	NP_001361707.1:p.Cys294Trp