Canonical Allele Identifier: CA402538850

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55217962G>C (hg19) ; chr18:g.57550730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550730G>C , CM000680.2:g.57550730G>C	GRCh38
NC_000018.9:g.55217962G>C , CM000680.1:g.55217962G>C	GRCh37
NC_000018.8:g.53368960G>C	NCBI36
NG_008175.1:g.41008C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1254C>G MANE Select	ENSP00000262093.6:p.Phe418Leu
ENST00000382873.8:c.1038C>G	ENSP00000372326.4:p.Phe346Leu
ENST00000651787.1:n.1360C>G
ENST00000652755.1:c.1272C>G	ENSP00000498358.1:p.Phe424Leu
ENST00000262093.9:c.1254C>G	ENSP00000262093.5:p.Phe418Leu
ENST00000382873.7:c.1272C>G	ENSP00000372326.3:p.Phe424Leu
ENST00000585494.5:c.*981C>G	ENSP00000465243.1:n.*981C>G
NM_000140.3:c.1254C>G	NP_000131.2:p.Phe418Leu
NM_001012515.2:c.1272C>G	NP_001012533.1:p.Phe424Leu
XM_011525881.1:c.1173C>G	XP_011524183.1:p.Phe391Leu
XM_011525882.1:c.1038C>G	XP_011524184.1:p.Phe346Leu
NM_000140.4:c.1254C>G	NP_000131.2:p.Phe418Leu
NM_001012515.3:c.1272C>G	NP_001012533.1:p.Phe424Leu
XM_011525882.2:c.1038C>G	XP_011524184.1:p.Phe346Leu
XM_017025614.2:c.1155C>G	XP_016881103.1:p.Phe385Leu
NM_000140.5:c.1254C>G MANE Select	NP_000131.2:p.Phe418Leu
NM_001012515.4:c.1272C>G	NP_001012533.1:p.Phe424Leu
NM_001371094.1:c.1155C>G	NP_001358023.1:p.Phe385Leu
NM_001371095.1:c.1038C>G	NP_001358024.1:p.Phe346Leu
NM_001374778.1:c.1194C>G	NP_001361707.1:p.Phe398Leu