Canonical Allele Identifier: CA2641939643
Gene: FECH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57550755_57550778del , CM000680.2:g.57550755_57550778del GRCh38
NC_000018.9:g.55217987_55218010del , CM000680.1:g.55217987_55218010del GRCh37
NC_000018.8:g.53368985_53369008del NCBI36
NG_008175.1:g.40963_40986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262093.11:c.1209_1232del MANE Select ENSP00000262093.6:p.Pro404_Cys411del
ENST00000382873.8:c.993_1016del ENSP00000372326.4:p.Pro332_Cys339del
ENST00000651787.1:n.1315_1338del
ENST00000652755.1:c.1227_1250del ENSP00000498358.1:p.Pro410_Cys417del
ENST00000262093.9:c.1209_1232del ENSP00000262093.5:p.Pro404_Cys411del
ENST00000382873.7:c.1227_1250del ENSP00000372326.3:p.Pro410_Cys417del
ENST00000585494.5:c.*936_*959del ENSP00000465243.1:n.*936_*959del
NM_000140.3:c.1209_1232del NP_000131.2:p.Pro404_Cys411del
NM_001012515.2:c.1227_1250del NP_001012533.1:p.Pro410_Cys417del
XM_011525881.1:c.1128_1151del XP_011524183.1:p.Pro377_Cys384del
XM_011525882.1:c.993_1016del XP_011524184.1:p.Pro332_Cys339del
NM_000140.4:c.1209_1232del NP_000131.2:p.Pro404_Cys411del
NM_001012515.3:c.1227_1250del NP_001012533.1:p.Pro410_Cys417del
XM_011525882.2:c.993_1016del XP_011524184.1:p.Pro332_Cys339del
XM_017025614.2:c.1110_1133del XP_016881103.1:p.Pro371_Cys378del
NM_000140.5:c.1209_1232del MANE Select NP_000131.2:p.Pro404_Cys411del
NM_001012515.4:c.1227_1250del NP_001012533.1:p.Pro410_Cys417del
NM_001371094.1:c.1110_1133del NP_001358023.1:p.Pro371_Cys378del
NM_001371095.1:c.993_1016del NP_001358024.1:p.Pro332_Cys339del
NM_001374778.1:c.1149_1172del NP_001361707.1:p.Pro384_Cys391del