Canonical Allele Identifier: CA504012732

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222140A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554908A>G , CM000680.2:g.57554908A>G	GRCh38
NC_000018.9:g.55222140A>G , CM000680.1:g.55222140A>G	GRCh37
NC_000018.8:g.53373138A>G	NCBI36
NG_008175.1:g.36830T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.750T>C	ENSP00000466263.1:p.Thr250=
ENST00000682485.1:n.1024T>C
ENST00000262093.11:c.849T>C MANE Select	ENSP00000262093.6:p.Thr283=
ENST00000382873.8:c.633T>C	ENSP00000372326.4:p.Thr211=
ENST00000651787.1:n.955T>C
ENST00000651812.1:n.446T>C
ENST00000652755.1:c.867T>C	ENSP00000498358.1:p.Thr289=
ENST00000262093.9:c.849T>C	ENSP00000262093.5:p.Thr283=
ENST00000382873.7:c.867T>C	ENSP00000372326.3:p.Thr289=
ENST00000585494.5:c.*576T>C	ENSP00000465243.1:n.*576T>C
ENST00000591977.5:c.116T>C
ENST00000592699.5:c.750T>C	ENSP00000466263.1:p.Thr250=
NM_000140.3:c.849T>C	NP_000131.2:p.Thr283=
NM_001012515.2:c.867T>C	NP_001012533.1:p.Thr289=
XM_011525881.1:c.768T>C	XP_011524183.1:p.Thr256=
XM_011525882.1:c.633T>C	XP_011524184.1:p.Thr211=
NM_000140.4:c.849T>C	NP_000131.2:p.Thr283=
NM_001012515.3:c.867T>C	NP_001012533.1:p.Thr289=
XM_011525882.2:c.633T>C	XP_011524184.1:p.Thr211=
XM_017025614.2:c.750T>C	XP_016881103.1:p.Thr250=
NM_000140.5:c.849T>C MANE Select	NP_000131.2:p.Thr283=
NM_001012515.4:c.867T>C	NP_001012533.1:p.Thr289=
NM_001371094.1:c.750T>C	NP_001358023.1:p.Thr250=
NM_001371095.1:c.633T>C	NP_001358024.1:p.Thr211=
NM_001374778.1:c.849T>C	NP_001361707.1:p.Thr283=