Canonical Allele Identifier: CA402538916
Gene: FECH HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.55217992A>C (hg19) chr18:g.57550760A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57550760A>C , CM000680.2:g.57550760A>C GRCh38
NC_000018.9:g.55217992A>C , CM000680.1:g.55217992A>C GRCh37
NC_000018.8:g.53368990A>C NCBI36
NG_008175.1:g.40978T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262093.11:c.1224T>G MANE Select ENSP00000262093.6:p.Asn408Lys
ENST00000382873.8:c.1008T>G ENSP00000372326.4:p.Asn336Lys
ENST00000651787.1:n.1330T>G
ENST00000652755.1:c.1242T>G ENSP00000498358.1:p.Asn414Lys
ENST00000262093.9:c.1224T>G ENSP00000262093.5:p.Asn408Lys
ENST00000382873.7:c.1242T>G ENSP00000372326.3:p.Asn414Lys
ENST00000585494.5:c.*951T>G ENSP00000465243.1:n.*951T>G
NM_000140.3:c.1224T>G NP_000131.2:p.Asn408Lys
NM_001012515.2:c.1242T>G NP_001012533.1:p.Asn414Lys
XM_011525881.1:c.1143T>G XP_011524183.1:p.Asn381Lys
XM_011525882.1:c.1008T>G XP_011524184.1:p.Asn336Lys
NM_000140.4:c.1224T>G NP_000131.2:p.Asn408Lys
NM_001012515.3:c.1242T>G NP_001012533.1:p.Asn414Lys
XM_011525882.2:c.1008T>G XP_011524184.1:p.Asn336Lys
XM_017025614.2:c.1125T>G XP_016881103.1:p.Asn375Lys
NM_000140.5:c.1224T>G MANE Select NP_000131.2:p.Asn408Lys
NM_001012515.4:c.1242T>G NP_001012533.1:p.Asn414Lys
NM_001371094.1:c.1125T>G NP_001358023.1:p.Asn375Lys
NM_001371095.1:c.1008T>G NP_001358024.1:p.Asn336Lys
NM_001374778.1:c.1164T>G NP_001361707.1:p.Asn388Lys
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