Canonical Allele Identifier: CA8973261

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573273C>T , CM000680.2:g.57573273C>T	GRCh38
NC_000018.9:g.55240505C>T , CM000680.1:g.55240505C>T	GRCh37
NC_000018.8:g.53391503C>T	NCBI36
NG_008175.1:g.18465G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000140.5:c.287G>A MANE Select	NP_000131.2:p.Arg96Gln
ENST00000262093.11:c.287G>A MANE Select	ENSP00000262093.6:p.Arg96Gln
NM_000140.3:c.287G>A	NP_000131.2:p.Arg96Gln
NM_000140.4:c.287G>A	NP_000131.2:p.Arg96Gln
NM_001012515.2:c.305G>A	NP_001012533.1:p.Arg102Gln
NM_001012515.3:c.305G>A	NP_001012533.1:p.Arg102Gln
NM_001012515.4:c.305G>A	NP_001012533.1:p.Arg102Gln
NM_001371094.1:c.287G>A	NP_001358023.1:p.Arg96Gln
NM_001371095.1:c.71G>A	NP_001358024.1:p.Arg24Gln
NM_001374778.1:c.287G>A	NP_001361707.1:p.Arg96Gln
ENST00000262093.9:c.287G>A	ENSP00000262093.5:p.Arg96Gln
ENST00000382873.7:c.305G>A	ENSP00000372326.3:p.Arg102Gln
ENST00000382873.8:c.71G>A	ENSP00000372326.4:p.Arg24Gln
ENST00000585494.5:c.287G>A	ENSP00000465243.1:p.Arg96Gln
ENST00000585699.1:n.239G>A
ENST00000585747.1:c.287G>A	ENSP00000465717.1:p.Arg96Gln
ENST00000585878.1:n.339G>A
ENST00000591215.5:c.71G>A	ENSP00000467461.1:p.Arg24Gln
ENST00000592111.1:n.288G>A
ENST00000592699.5:c.287G>A	ENSP00000466263.1:p.Arg96Gln
ENST00000592699.6:c.287G>A	ENSP00000466263.1:p.Arg96Gln
ENST00000651787.1:n.393G>A
ENST00000652755.1:c.305G>A	ENSP00000498358.1:p.Arg102Gln
ENST00000682485.1:n.399G>A
XM_011525881.1:c.305G>A	XP_011524183.1:p.Arg102Gln
XM_011525882.1:c.71G>A	XP_011524184.1:p.Arg24Gln
XM_011525882.2:c.71G>A	XP_011524184.1:p.Arg24Gln
XM_017025614.2:c.287G>A	XP_016881103.1:p.Arg96Gln