Canonical Allele Identifier: CA504010291

Gene: FECH

Linked Data

• dbSNP Id: rs1351124222
• gnomAD v2: 18-55240480-C-T
• gnomAD v4: 18-57573248-C-T
• MyVariant Identifiers: chr18:g.55240480C>T (hg19) ; chr18:g.57573248C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573248C>T , CM000680.2:g.57573248C>T	GRCh38
NC_000018.9:g.55240480C>T , CM000680.1:g.55240480C>T	GRCh37
NC_000018.8:g.53391478C>T	NCBI36
NG_008175.1:g.18490G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.312G>A	ENSP00000466263.1:p.Gln104=
ENST00000682485.1:n.424G>A
ENST00000262093.11:c.312G>A MANE Select	ENSP00000262093.6:p.Gln104=
ENST00000382873.8:c.96G>A	ENSP00000372326.4:p.Gln32=
ENST00000651787.1:n.418G>A
ENST00000652755.1:c.330G>A	ENSP00000498358.1:p.Gln110=
ENST00000262093.9:c.312G>A	ENSP00000262093.5:p.Gln104=
ENST00000382873.7:c.330G>A	ENSP00000372326.3:p.Gln110=
ENST00000585494.5:c.312G>A	ENSP00000465243.1:p.Gln104=
ENST00000585699.1:n.264G>A
ENST00000585747.1:c.312G>A	ENSP00000465717.1:p.Gln104=
ENST00000585878.1:n.364G>A
ENST00000591215.5:c.96G>A	ENSP00000467461.1:p.Gln32=
ENST00000592111.1:n.313G>A
ENST00000592699.5:c.312G>A	ENSP00000466263.1:p.Gln104=
NM_000140.3:c.312G>A	NP_000131.2:p.Gln104=
NM_001012515.2:c.330G>A	NP_001012533.1:p.Gln110=
XM_011525881.1:c.330G>A	XP_011524183.1:p.Gln110=
XM_011525882.1:c.96G>A	XP_011524184.1:p.Gln32=
NM_000140.4:c.312G>A	NP_000131.2:p.Gln104=
NM_001012515.3:c.330G>A	NP_001012533.1:p.Gln110=
XM_011525882.2:c.96G>A	XP_011524184.1:p.Gln32=
XM_017025614.2:c.312G>A	XP_016881103.1:p.Gln104=
NM_000140.5:c.312G>A MANE Select	NP_000131.2:p.Gln104=
NM_001012515.4:c.330G>A	NP_001012533.1:p.Gln110=
NM_001371094.1:c.312G>A	NP_001358023.1:p.Gln104=
NM_001371095.1:c.96G>A	NP_001358024.1:p.Gln32=
NM_001374778.1:c.312G>A	NP_001361707.1:p.Gln104=