Canonical Allele Identifier: CA504012735

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222143G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554911G>T , CM000680.2:g.57554911G>T	GRCh38
NC_000018.9:g.55222143G>T , CM000680.1:g.55222143G>T	GRCh37
NC_000018.8:g.53373141G>T	NCBI36
NG_008175.1:g.36827C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.747C>A	ENSP00000466263.1:p.Ala249=
ENST00000682485.1:n.1021C>A
ENST00000262093.11:c.846C>A MANE Select	ENSP00000262093.6:p.Ala282=
ENST00000382873.8:c.630C>A	ENSP00000372326.4:p.Ala210=
ENST00000651787.1:n.952C>A
ENST00000651812.1:n.443C>A
ENST00000652755.1:c.864C>A	ENSP00000498358.1:p.Ala288=
ENST00000262093.9:c.846C>A	ENSP00000262093.5:p.Ala282=
ENST00000382873.7:c.864C>A	ENSP00000372326.3:p.Ala288=
ENST00000585494.5:c.*573C>A	ENSP00000465243.1:n.*573C>A
ENST00000591977.5:c.113C>A
ENST00000592699.5:c.747C>A	ENSP00000466263.1:p.Ala249=
NM_000140.3:c.846C>A	NP_000131.2:p.Ala282=
NM_001012515.2:c.864C>A	NP_001012533.1:p.Ala288=
XM_011525881.1:c.765C>A	XP_011524183.1:p.Ala255=
XM_011525882.1:c.630C>A	XP_011524184.1:p.Ala210=
NM_000140.4:c.846C>A	NP_000131.2:p.Ala282=
NM_001012515.3:c.864C>A	NP_001012533.1:p.Ala288=
XM_011525882.2:c.630C>A	XP_011524184.1:p.Ala210=
XM_017025614.2:c.747C>A	XP_016881103.1:p.Ala249=
NM_000140.5:c.846C>A MANE Select	NP_000131.2:p.Ala282=
NM_001012515.4:c.864C>A	NP_001012533.1:p.Ala288=
NM_001371094.1:c.747C>A	NP_001358023.1:p.Ala249=
NM_001371095.1:c.630C>A	NP_001358024.1:p.Ala210=
NM_001374778.1:c.846C>A	NP_001361707.1:p.Ala282=