Canonical Allele Identifier: CA402536921

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55240528G>T (hg19) ; chr18:g.57573296G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573296G>T , CM000680.2:g.57573296G>T	GRCh38
NC_000018.9:g.55240528G>T , CM000680.1:g.55240528G>T	GRCh37
NC_000018.8:g.53391526G>T	NCBI36
NG_008175.1:g.18442C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.264C>A	ENSP00000466263.1:p.Phe88Leu
ENST00000682485.1:n.376C>A
ENST00000262093.11:c.264C>A MANE Select	ENSP00000262093.6:p.Phe88Leu
ENST00000382873.8:c.48C>A	ENSP00000372326.4:p.Phe16Leu
ENST00000651787.1:n.370C>A
ENST00000652755.1:c.282C>A	ENSP00000498358.1:p.Phe94Leu
ENST00000262093.9:c.264C>A	ENSP00000262093.5:p.Phe88Leu
ENST00000382873.7:c.282C>A	ENSP00000372326.3:p.Phe94Leu
ENST00000585494.5:c.264C>A	ENSP00000465243.1:p.Phe88Leu
ENST00000585699.1:n.216C>A
ENST00000585747.1:c.264C>A	ENSP00000465717.1:p.Phe88Leu
ENST00000585878.1:n.316C>A
ENST00000591215.5:c.48C>A	ENSP00000467461.1:p.Phe16Leu
ENST00000592111.1:n.265C>A
ENST00000592699.5:c.264C>A	ENSP00000466263.1:p.Phe88Leu
NM_000140.3:c.264C>A	NP_000131.2:p.Phe88Leu
NM_001012515.2:c.282C>A	NP_001012533.1:p.Phe94Leu
XM_011525881.1:c.282C>A	XP_011524183.1:p.Phe94Leu
XM_011525882.1:c.48C>A	XP_011524184.1:p.Phe16Leu
NM_000140.4:c.264C>A	NP_000131.2:p.Phe88Leu
NM_001012515.3:c.282C>A	NP_001012533.1:p.Phe94Leu
XM_011525882.2:c.48C>A	XP_011524184.1:p.Phe16Leu
XM_017025614.2:c.264C>A	XP_016881103.1:p.Phe88Leu
NM_000140.5:c.264C>A MANE Select	NP_000131.2:p.Phe88Leu
NM_001012515.4:c.282C>A	NP_001012533.1:p.Phe94Leu
NM_001371094.1:c.264C>A	NP_001358023.1:p.Phe88Leu
NM_001371095.1:c.48C>A	NP_001358024.1:p.Phe16Leu
NM_001374778.1:c.264C>A	NP_001361707.1:p.Phe88Leu