Canonical Allele Identifier: CA2306047338
Gene: FECH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57554208A= , CM000680.2:g.57554208A= GRCh38
NC_000018.9:g.55221440A= , CM000680.1:g.55221440A= GRCh37
NC_000018.8:g.53372438A= NCBI36
NG_008175.1:g.37530T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682485.1:n.1304T=
ENST00000262093.11:c.1077+52T= MANE Select ENSP00000262093.6:n.1077+52T=
ENST00000382873.8:c.861+52T= ENSP00000372326.4:n.861+52T=
ENST00000651787.1:n.1183+52T=
ENST00000652755.1:c.1095+52T= ENSP00000498358.1:n.1095+52T=
ENST00000262093.9:c.1077+52T= ENSP00000262093.5:n.1077+52T=
ENST00000382873.7:c.1095+52T= ENSP00000372326.3:n.1095+52T=
ENST00000585494.5:c.*804+52T= ENSP00000465243.1:n.*804+52T=
ENST00000591977.5:c.344+52T=
NM_000140.3:c.1077+52T= NP_000131.2:n.1077+52T=
NM_001012515.2:c.1095+52T= NP_001012533.1:n.1095+52T=
XM_011525881.1:c.996+52T= XP_011524183.1:n.996+52T=
XM_011525882.1:c.861+52T= XP_011524184.1:n.861+52T=
NM_000140.4:c.1077+52T= NP_000131.2:n.1077+52T=
NM_001012515.3:c.1095+52T= NP_001012533.1:n.1095+52T=
XM_011525882.2:c.861+52T= XP_011524184.1:n.861+52T=
XM_017025614.2:c.978+52T= XP_016881103.1:n.978+52T=
NM_000140.5:c.1077+52T= MANE Select NP_000131.2:n.1077+52T=
NM_001012515.4:c.1095+52T= NP_001012533.1:n.1095+52T=
NM_001371094.1:c.978+52T= NP_001358023.1:n.978+52T=
NM_001371095.1:c.861+52T= NP_001358024.1:n.861+52T=
NM_001374778.1:c.1077+52T= NP_001361707.1:n.1077+52T=