Canonical Allele Identifier: CA2306045859
Gene: FECH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57550571C= , CM000680.2:g.57550571C= GRCh38
NC_000018.9:g.55217803C= , CM000680.1:g.55217803C= GRCh37
NC_000018.8:g.53368801C= NCBI36
NG_008175.1:g.41167G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262093.11:c.*141G= MANE Select ENSP00000262093.6:n.*141G=
ENST00000382873.8:c.*141G= ENSP00000372326.4:n.*141G=
ENST00000651787.1:n.1519G=
ENST00000652755.1:c.*141G= ENSP00000498358.1:n.*141G=
ENST00000262093.9:c.*141G= ENSP00000262093.5:n.*141G=
ENST00000382873.7:c.*141G= ENSP00000372326.3:n.*141G=
ENST00000585494.5:c.*1140G= ENSP00000465243.1:n.*1140G=
NM_000140.3:c.*141G= NP_000131.2:n.*141G=
NM_001012515.2:c.*141G= NP_001012533.1:n.*141G=
XM_011525881.1:c.*141G= XP_011524183.1:n.*141G=
XM_011525882.1:c.*141G= XP_011524184.1:n.*141G=
NM_000140.4:c.*141G= NP_000131.2:n.*141G=
NM_001012515.3:c.*141G= NP_001012533.1:n.*141G=
XM_011525882.2:c.*141G= XP_011524184.1:n.*141G=
XM_017025614.2:c.*141G= XP_016881103.1:n.*141G=
NM_000140.5:c.*141G= MANE Select NP_000131.2:n.*141G=
NM_001012515.4:c.*141G= NP_001012533.1:n.*141G=
NM_001371094.1:c.*141G= NP_001358023.1:n.*141G=
NM_001371095.1:c.*141G= NP_001358024.1:n.*141G=
NM_001374778.1:c.*141G= NP_001361707.1:n.*141G=