Canonical Allele Identifier: CA504011562

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55217992A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1224T>C MANE Select	ENSP00000262093.6:p.Asn408=
ENST00000382873.8:c.1008T>C	ENSP00000372326.4:p.Asn336=
ENST00000651787.1:n.1330T>C
ENST00000652755.1:c.1242T>C	ENSP00000498358.1:p.Asn414=
ENST00000262093.9:c.1224T>C	ENSP00000262093.5:p.Asn408=
ENST00000382873.7:c.1242T>C	ENSP00000372326.3:p.Asn414=
ENST00000585494.5:c.*951T>C	ENSP00000465243.1:n.*951T>C
NM_000140.3:c.1224T>C	NP_000131.2:p.Asn408=
NM_001012515.2:c.1242T>C	NP_001012533.1:p.Asn414=
XM_011525881.1:c.1143T>C	XP_011524183.1:p.Asn381=
XM_011525882.1:c.1008T>C	XP_011524184.1:p.Asn336=
NM_000140.4:c.1224T>C	NP_000131.2:p.Asn408=
NM_001012515.3:c.1242T>C	NP_001012533.1:p.Asn414=
XM_011525882.2:c.1008T>C	XP_011524184.1:p.Asn336=
XM_017025614.2:c.1125T>C	XP_016881103.1:p.Asn375=
NM_000140.5:c.1224T>C MANE Select	NP_000131.2:p.Asn408=
NM_001012515.4:c.1242T>C	NP_001012533.1:p.Asn414=
NM_001371094.1:c.1125T>C	NP_001358023.1:p.Asn375=
NM_001371095.1:c.1008T>C	NP_001358024.1:p.Asn336=
NM_001374778.1:c.1164T>C	NP_001361707.1:p.Asn388=