Canonical Allele Identifier: CA504012655
Gene: FECH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57554615_57554616del , CM000680.2:g.57554615_57554616del GRCh38
NC_000018.9:g.55221847_55221848del , CM000680.1:g.55221847_55221848del GRCh37
NC_000018.8:g.53372845_53372846del NCBI36
NG_008175.1:g.37123_37124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000592699.6:c.814-191_814-190del ENSP00000466263.1:n.814-191_814-190del
ENST00000682485.1:n.1088-191_1088-190del
ENST00000262093.11:c.913-191_913-190del MANE Select ENSP00000262093.6:n.913-191_913-190del
ENST00000382873.8:c.697-191_697-190del ENSP00000372326.4:n.697-191_697-190del
ENST00000651787.1:n.1019-191_1019-190del
ENST00000651812.1:n.510-191_510-190del
ENST00000652755.1:c.931-191_931-190del ENSP00000498358.1:n.931-191_931-190del
ENST00000262093.9:c.913-191_913-190del ENSP00000262093.5:n.913-191_913-190del
ENST00000382873.7:c.931-191_931-190del ENSP00000372326.3:n.931-191_931-190del
ENST00000585494.5:c.*640-191_*640-190del ENSP00000465243.1:n.*640-191_*640-190del
ENST00000591977.5:c.180-191_180-190del
ENST00000592699.5:c.814-191_814-190del ENSP00000466263.1:n.814-191_814-190del
NM_000140.3:c.913-191_913-190del NP_000131.2:n.913-191_913-190del
NM_001012515.2:c.931-191_931-190del NP_001012533.1:n.931-191_931-190del
XM_011525881.1:c.832-191_832-190del XP_011524183.1:n.832-191_832-190del
XM_011525882.1:c.697-191_697-190del XP_011524184.1:n.697-191_697-190del
NM_000140.4:c.913-191_913-190del NP_000131.2:n.913-191_913-190del
NM_001012515.3:c.931-191_931-190del NP_001012533.1:n.931-191_931-190del
XM_011525882.2:c.697-191_697-190del XP_011524184.1:n.697-191_697-190del
XM_017025614.2:c.814-191_814-190del XP_016881103.1:n.814-191_814-190del
NM_000140.5:c.913-191_913-190del MANE Select NP_000131.2:n.913-191_913-190del
NM_001012515.4:c.931-191_931-190del NP_001012533.1:n.931-191_931-190del
NM_001371094.1:c.814-191_814-190del NP_001358023.1:n.814-191_814-190del
NM_001371095.1:c.697-191_697-190del NP_001358024.1:n.697-191_697-190del
NM_001374778.1:c.913-191_913-190del NP_001361707.1:n.913-191_913-190del