Canonical Allele Identifier: CA402536883

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55240518G>C (hg19) ; chr18:g.57573286G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573286G>C , CM000680.2:g.57573286G>C	GRCh38
NC_000018.9:g.55240518G>C , CM000680.1:g.55240518G>C	GRCh37
NC_000018.8:g.53391516G>C	NCBI36
NG_008175.1:g.18452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.274C>G	ENSP00000466263.1:p.Leu92Val
ENST00000682485.1:n.386C>G
ENST00000262093.11:c.274C>G MANE Select	ENSP00000262093.6:p.Leu92Val
ENST00000382873.8:c.58C>G	ENSP00000372326.4:p.Leu20Val
ENST00000651787.1:n.380C>G
ENST00000652755.1:c.292C>G	ENSP00000498358.1:p.Leu98Val
ENST00000262093.9:c.274C>G	ENSP00000262093.5:p.Leu92Val
ENST00000382873.7:c.292C>G	ENSP00000372326.3:p.Leu98Val
ENST00000585494.5:c.274C>G	ENSP00000465243.1:p.Leu92Val
ENST00000585699.1:n.226C>G
ENST00000585747.1:c.274C>G	ENSP00000465717.1:p.Leu92Val
ENST00000585878.1:n.326C>G
ENST00000591215.5:c.58C>G	ENSP00000467461.1:p.Leu20Val
ENST00000592111.1:n.275C>G
ENST00000592699.5:c.274C>G	ENSP00000466263.1:p.Leu92Val
NM_000140.3:c.274C>G	NP_000131.2:p.Leu92Val
NM_001012515.2:c.292C>G	NP_001012533.1:p.Leu98Val
XM_011525881.1:c.292C>G	XP_011524183.1:p.Leu98Val
XM_011525882.1:c.58C>G	XP_011524184.1:p.Leu20Val
NM_000140.4:c.274C>G	NP_000131.2:p.Leu92Val
NM_001012515.3:c.292C>G	NP_001012533.1:p.Leu98Val
XM_011525882.2:c.58C>G	XP_011524184.1:p.Leu20Val
XM_017025614.2:c.274C>G	XP_016881103.1:p.Leu92Val
NM_000140.5:c.274C>G MANE Select	NP_000131.2:p.Leu92Val
NM_001012515.4:c.292C>G	NP_001012533.1:p.Leu98Val
NM_001371094.1:c.274C>G	NP_001358023.1:p.Leu92Val
NM_001371095.1:c.58C>G	NP_001358024.1:p.Leu20Val
NM_001374778.1:c.274C>G	NP_001361707.1:p.Leu92Val