Canonical Allele Identifier: CA402536798

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55240479T>G (hg19) ; chr18:g.57573247T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573247T>G , CM000680.2:g.57573247T>G	GRCh38
NC_000018.9:g.55240479T>G , CM000680.1:g.55240479T>G	GRCh37
NC_000018.8:g.53391477T>G	NCBI36
NG_008175.1:g.18491A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.313A>C	ENSP00000466263.1:p.Asn105His
ENST00000682485.1:n.425A>C
ENST00000262093.11:c.313A>C MANE Select	ENSP00000262093.6:p.Asn105His
ENST00000382873.8:c.97A>C	ENSP00000372326.4:p.Asn33His
ENST00000651787.1:n.419A>C
ENST00000652755.1:c.331A>C	ENSP00000498358.1:p.Asn111His
ENST00000262093.9:c.313A>C	ENSP00000262093.5:p.Asn105His
ENST00000382873.7:c.331A>C	ENSP00000372326.3:p.Asn111His
ENST00000585494.5:c.313A>C	ENSP00000465243.1:p.Lys105Gln
ENST00000585699.1:n.265A>C
ENST00000585747.1:c.313A>C	ENSP00000465717.1:p.Asn105His
ENST00000585878.1:n.365A>C
ENST00000591215.5:c.97A>C	ENSP00000467461.1:p.Asn33His
ENST00000592111.1:n.314A>C
ENST00000592699.5:c.313A>C	ENSP00000466263.1:p.Asn105His
NM_000140.3:c.313A>C	NP_000131.2:p.Asn105His
NM_001012515.2:c.331A>C	NP_001012533.1:p.Asn111His
XM_011525881.1:c.331A>C	XP_011524183.1:p.Asn111His
XM_011525882.1:c.97A>C	XP_011524184.1:p.Asn33His
NM_000140.4:c.313A>C	NP_000131.2:p.Asn105His
NM_001012515.3:c.331A>C	NP_001012533.1:p.Asn111His
XM_011525882.2:c.97A>C	XP_011524184.1:p.Asn33His
XM_017025614.2:c.313A>C	XP_016881103.1:p.Asn105His
NM_000140.5:c.313A>C MANE Select	NP_000131.2:p.Asn105His
NM_001012515.4:c.331A>C	NP_001012533.1:p.Asn111His
NM_001371094.1:c.313A>C	NP_001358023.1:p.Asn105His
NM_001371095.1:c.97A>C	NP_001358024.1:p.Asn33His
NM_001374778.1:c.313A>C	NP_001361707.1:p.Asn105His