Canonical Allele Identifier: CA504012718

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222116C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554884C>G , CM000680.2:g.57554884C>G	GRCh38
NC_000018.9:g.55222116C>G , CM000680.1:g.55222116C>G	GRCh37
NC_000018.8:g.53373114C>G	NCBI36
NG_008175.1:g.36854G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.774G>C	ENSP00000466263.1:p.Leu258=
ENST00000682485.1:n.1048G>C
ENST00000262093.11:c.873G>C MANE Select	ENSP00000262093.6:p.Leu291=
ENST00000382873.8:c.657G>C	ENSP00000372326.4:p.Leu219=
ENST00000651787.1:n.979G>C
ENST00000651812.1:n.470G>C
ENST00000652755.1:c.891G>C	ENSP00000498358.1:p.Leu297=
ENST00000262093.9:c.873G>C	ENSP00000262093.5:p.Leu291=
ENST00000382873.7:c.891G>C	ENSP00000372326.3:p.Leu297=
ENST00000585494.5:c.*600G>C	ENSP00000465243.1:n.*600G>C
ENST00000591977.5:c.140G>C
ENST00000592699.5:c.774G>C	ENSP00000466263.1:p.Leu258=
NM_000140.3:c.873G>C	NP_000131.2:p.Leu291=
NM_001012515.2:c.891G>C	NP_001012533.1:p.Leu297=
XM_011525881.1:c.792G>C	XP_011524183.1:p.Leu264=
XM_011525882.1:c.657G>C	XP_011524184.1:p.Leu219=
NM_000140.4:c.873G>C	NP_000131.2:p.Leu291=
NM_001012515.3:c.891G>C	NP_001012533.1:p.Leu297=
XM_011525882.2:c.657G>C	XP_011524184.1:p.Leu219=
XM_017025614.2:c.774G>C	XP_016881103.1:p.Leu258=
NM_000140.5:c.873G>C MANE Select	NP_000131.2:p.Leu291=
NM_001012515.4:c.891G>C	NP_001012533.1:p.Leu297=
NM_001371094.1:c.774G>C	NP_001358023.1:p.Leu258=
NM_001371095.1:c.657G>C	NP_001358024.1:p.Leu219=
NM_001374778.1:c.873G>C	NP_001361707.1:p.Leu291=