Canonical Allele Identifier: CA402541344

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55222138A>T (hg19) ; chr18:g.57554906A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554906A>T , CM000680.2:g.57554906A>T	GRCh38
NC_000018.9:g.55222138A>T , CM000680.1:g.55222138A>T	GRCh37
NC_000018.8:g.53373136A>T	NCBI36
NG_008175.1:g.36832T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.752T>A	ENSP00000466263.1:p.Val251Asp
ENST00000682485.1:n.1026T>A
ENST00000262093.11:c.851T>A MANE Select	ENSP00000262093.6:p.Val284Asp
ENST00000382873.8:c.635T>A	ENSP00000372326.4:p.Val212Asp
ENST00000651787.1:n.957T>A
ENST00000651812.1:n.448T>A
ENST00000652755.1:c.869T>A	ENSP00000498358.1:p.Val290Asp
ENST00000262093.9:c.851T>A	ENSP00000262093.5:p.Val284Asp
ENST00000382873.7:c.869T>A	ENSP00000372326.3:p.Val290Asp
ENST00000585494.5:c.*578T>A	ENSP00000465243.1:n.*578T>A
ENST00000591977.5:c.118T>A
ENST00000592699.5:c.752T>A	ENSP00000466263.1:p.Val251Asp
NM_000140.3:c.851T>A	NP_000131.2:p.Val284Asp
NM_001012515.2:c.869T>A	NP_001012533.1:p.Val290Asp
XM_011525881.1:c.770T>A	XP_011524183.1:p.Val257Asp
XM_011525882.1:c.635T>A	XP_011524184.1:p.Val212Asp
NM_000140.4:c.851T>A	NP_000131.2:p.Val284Asp
NM_001012515.3:c.869T>A	NP_001012533.1:p.Val290Asp
XM_011525882.2:c.635T>A	XP_011524184.1:p.Val212Asp
XM_017025614.2:c.752T>A	XP_016881103.1:p.Val251Asp
NM_000140.5:c.851T>A MANE Select	NP_000131.2:p.Val284Asp
NM_001012515.4:c.869T>A	NP_001012533.1:p.Val290Asp
NM_001371094.1:c.752T>A	NP_001358023.1:p.Val251Asp
NM_001371095.1:c.635T>A	NP_001358024.1:p.Val212Asp
NM_001374778.1:c.851T>A	NP_001361707.1:p.Val284Asp