Canonical Allele Identifier: CA402537028
Gene: FECH HGNC NCBI

Linked Data

dbSNP Id: rs1449360770

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57573327C>G , CM000680.2:g.57573327C>G GRCh38
NC_000018.9:g.55240559C>G , CM000680.1:g.55240559C>G GRCh37
NC_000018.8:g.53391557C>G NCBI36
NG_008175.1:g.18411G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000592699.6:c.233G>C ENSP00000466263.1:p.Gly78Ala
ENST00000682485.1:n.345G>C
ENST00000262093.11:c.233G>C MANE Select ENSP00000262093.6:p.Gly78Ala
ENST00000382873.8:c.17G>C ENSP00000372326.4:p.Gly6Ala
ENST00000651787.1:n.339G>C
ENST00000652755.1:c.251G>C ENSP00000498358.1:p.Gly84Ala
ENST00000262093.9:c.233G>C ENSP00000262093.5:p.Gly78Ala
ENST00000382873.7:c.251G>C ENSP00000372326.3:p.Gly84Ala
ENST00000585494.5:c.233G>C ENSP00000465243.1:p.Gly78Ala
ENST00000585699.1:n.185G>C
ENST00000585747.1:c.233G>C ENSP00000465717.1:p.Gly78Ala
ENST00000585878.1:n.285G>C
ENST00000591215.5:c.17G>C ENSP00000467461.1:p.Gly6Ala
ENST00000592111.1:n.234G>C
ENST00000592699.5:c.233G>C ENSP00000466263.1:p.Gly78Ala
NM_000140.3:c.233G>C NP_000131.2:p.Gly78Ala
NM_001012515.2:c.251G>C NP_001012533.1:p.Gly84Ala
XM_011525881.1:c.251G>C XP_011524183.1:p.Gly84Ala
XM_011525882.1:c.17G>C XP_011524184.1:p.Gly6Ala
NM_000140.4:c.233G>C NP_000131.2:p.Gly78Ala
NM_001012515.3:c.251G>C NP_001012533.1:p.Gly84Ala
XM_011525882.2:c.17G>C XP_011524184.1:p.Gly6Ala
XM_017025614.2:c.233G>C XP_016881103.1:p.Gly78Ala
NM_000140.5:c.233G>C MANE Select NP_000131.2:p.Gly78Ala
NM_001012515.4:c.251G>C NP_001012533.1:p.Gly84Ala
NM_001371094.1:c.233G>C NP_001358023.1:p.Gly78Ala
NM_001371095.1:c.17G>C NP_001358024.1:p.Gly6Ala
NM_001374778.1:c.233G>C NP_001361707.1:p.Gly78Ala