Canonical Allele Identifier: CA402538836

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55217955G>C (hg19) ; chr18:g.57550723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550723G>C , CM000680.2:g.57550723G>C	GRCh38
NC_000018.9:g.55217955G>C , CM000680.1:g.55217955G>C	GRCh37
NC_000018.8:g.53368953G>C	NCBI36
NG_008175.1:g.41015C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1261C>G MANE Select	ENSP00000262093.6:p.Gln421Glu
ENST00000382873.8:c.1045C>G	ENSP00000372326.4:p.Gln349Glu
ENST00000651787.1:n.1367C>G
ENST00000652755.1:c.1279C>G	ENSP00000498358.1:p.Gln427Glu
ENST00000262093.9:c.1261C>G	ENSP00000262093.5:p.Gln421Glu
ENST00000382873.7:c.1279C>G	ENSP00000372326.3:p.Gln427Glu
ENST00000585494.5:c.*988C>G	ENSP00000465243.1:n.*988C>G
NM_000140.3:c.1261C>G	NP_000131.2:p.Gln421Glu
NM_001012515.2:c.1279C>G	NP_001012533.1:p.Gln427Glu
XM_011525881.1:c.1180C>G	XP_011524183.1:p.Gln394Glu
XM_011525882.1:c.1045C>G	XP_011524184.1:p.Gln349Glu
NM_000140.4:c.1261C>G	NP_000131.2:p.Gln421Glu
NM_001012515.3:c.1279C>G	NP_001012533.1:p.Gln427Glu
XM_011525882.2:c.1045C>G	XP_011524184.1:p.Gln349Glu
XM_017025614.2:c.1162C>G	XP_016881103.1:p.Gln388Glu
NM_000140.5:c.1261C>G MANE Select	NP_000131.2:p.Gln421Glu
NM_001012515.4:c.1279C>G	NP_001012533.1:p.Gln427Glu
NM_001371094.1:c.1162C>G	NP_001358023.1:p.Gln388Glu
NM_001371095.1:c.1045C>G	NP_001358024.1:p.Gln349Glu
NM_001374778.1:c.1201C>G	NP_001361707.1:p.Gln401Glu