Canonical Allele Identifier: CA630050593
Gene: FECH HGNC NCBI

Linked Data

dbSNP Id: rs1438566854

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57550599_57550603del , CM000680.2:g.57550599_57550603del GRCh38
NC_000018.9:g.55217831_55217835del , CM000680.1:g.55217831_55217835del GRCh37
NC_000018.8:g.53368829_53368833del NCBI36
NG_008175.1:g.41135_41139del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262093.11:c.*109_*113del MANE Select ENSP00000262093.6:n.*109_*113del
ENST00000382873.8:c.*109_*113del ENSP00000372326.4:n.*109_*113del
ENST00000651787.1:n.1487_1491del
ENST00000652755.1:c.*109_*113del ENSP00000498358.1:n.*109_*113del
ENST00000262093.9:c.*109_*113del ENSP00000262093.5:n.*109_*113del
ENST00000382873.7:c.*109_*113del ENSP00000372326.3:n.*109_*113del
ENST00000585494.5:c.*1108_*1112del ENSP00000465243.1:n.*1108_*1112del
NM_000140.3:c.*109_*113del NP_000131.2:n.*109_*113del
NM_001012515.2:c.*109_*113del NP_001012533.1:n.*109_*113del
XM_011525881.1:c.*109_*113del XP_011524183.1:n.*109_*113del
XM_011525882.1:c.*109_*113del XP_011524184.1:n.*109_*113del
NM_000140.4:c.*109_*113del NP_000131.2:n.*109_*113del
NM_001012515.3:c.*109_*113del NP_001012533.1:n.*109_*113del
XM_011525882.2:c.*109_*113del XP_011524184.1:n.*109_*113del
XM_017025614.2:c.*109_*113del XP_016881103.1:n.*109_*113del
NM_000140.5:c.*109_*113del MANE Select NP_000131.2:n.*109_*113del
NM_001012515.4:c.*109_*113del NP_001012533.1:n.*109_*113del
NM_001371094.1:c.*109_*113del NP_001358023.1:n.*109_*113del
NM_001371095.1:c.*109_*113del NP_001358024.1:n.*109_*113del
NM_001374778.1:c.*109_*113del NP_001361707.1:n.*109_*113del