Canonical Allele Identifier: CA300851744

Gene: FECH

Linked Data

• dbSNP Id: rs771195505
• gnomAD v3: 18-57550582-G-A
• gnomAD v4: 18-57550582-G-A
• MyVariant Identifiers: chr18:g.55217814G>A (hg19) ; chr18:g.57550582G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550582G>A , CM000680.2:g.57550582G>A	GRCh38
NC_000018.9:g.55217814G>A , CM000680.1:g.55217814G>A	GRCh37
NC_000018.8:g.53368812G>A	NCBI36
NG_008175.1:g.41156C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.*130C>T MANE Select	ENSP00000262093.6:n.*130C>T
ENST00000382873.8:c.*130C>T	ENSP00000372326.4:n.*130C>T
ENST00000651787.1:n.1508C>T
ENST00000652755.1:c.*130C>T	ENSP00000498358.1:n.*130C>T
ENST00000262093.9:c.*130C>T	ENSP00000262093.5:n.*130C>T
ENST00000382873.7:c.*130C>T	ENSP00000372326.3:n.*130C>T
ENST00000585494.5:c.*1129C>T	ENSP00000465243.1:n.*1129C>T
NM_000140.3:c.*130C>T	NP_000131.2:n.*130C>T
NM_001012515.2:c.*130C>T	NP_001012533.1:n.*130C>T
XM_011525881.1:c.*130C>T	XP_011524183.1:n.*130C>T
XM_011525882.1:c.*130C>T	XP_011524184.1:n.*130C>T
NM_000140.4:c.*130C>T	NP_000131.2:n.*130C>T
NM_001012515.3:c.*130C>T	NP_001012533.1:n.*130C>T
XM_011525882.2:c.*130C>T	XP_011524184.1:n.*130C>T
XM_017025614.2:c.*130C>T	XP_016881103.1:n.*130C>T
NM_000140.5:c.*130C>T MANE Select	NP_000131.2:n.*130C>T
NM_001012515.4:c.*130C>T	NP_001012533.1:n.*130C>T
NM_001371094.1:c.*130C>T	NP_001358023.1:n.*130C>T
NM_001371095.1:c.*130C>T	NP_001358024.1:n.*130C>T
NM_001374778.1:c.*130C>T	NP_001361707.1:n.*130C>T