Canonical Allele Identifier: CA402538882

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55217976T>A (hg19) ; chr18:g.57550744T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550744T>A , CM000680.2:g.57550744T>A	GRCh38
NC_000018.9:g.55217976T>A , CM000680.1:g.55217976T>A	GRCh37
NC_000018.8:g.53368974T>A	NCBI36
NG_008175.1:g.40994A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262093.11:c.1240A>T MANE Select	ENSP00000262093.6:p.Thr414Ser
ENST00000382873.8:c.1024A>T	ENSP00000372326.4:p.Thr342Ser
ENST00000651787.1:n.1346A>T
ENST00000652755.1:c.1258A>T	ENSP00000498358.1:p.Thr420Ser
ENST00000262093.9:c.1240A>T	ENSP00000262093.5:p.Thr414Ser
ENST00000382873.7:c.1258A>T	ENSP00000372326.3:p.Thr420Ser
ENST00000585494.5:c.*967A>T	ENSP00000465243.1:n.*967A>T
NM_000140.3:c.1240A>T	NP_000131.2:p.Thr414Ser
NM_001012515.2:c.1258A>T	NP_001012533.1:p.Thr420Ser
XM_011525881.1:c.1159A>T	XP_011524183.1:p.Thr387Ser
XM_011525882.1:c.1024A>T	XP_011524184.1:p.Thr342Ser
NM_000140.4:c.1240A>T	NP_000131.2:p.Thr414Ser
NM_001012515.3:c.1258A>T	NP_001012533.1:p.Thr420Ser
XM_011525882.2:c.1024A>T	XP_011524184.1:p.Thr342Ser
XM_017025614.2:c.1141A>T	XP_016881103.1:p.Thr381Ser
NM_000140.5:c.1240A>T MANE Select	NP_000131.2:p.Thr414Ser
NM_001012515.4:c.1258A>T	NP_001012533.1:p.Thr420Ser
NM_001371094.1:c.1141A>T	NP_001358023.1:p.Thr381Ser
NM_001371095.1:c.1024A>T	NP_001358024.1:p.Thr342Ser
NM_001374778.1:c.1180A>T	NP_001361707.1:p.Thr394Ser