Canonical Allele Identifier: CA10641839

Gene: FECH

Linked Data

• ClinVar Variation Id: 327420
• ClinVar RCV Id: RCV000303699
• dbSNP Id: rs886053995
• gnomAD v4: 18-57550576-C-G
• MyVariant Identifiers: chr18:g.55217808C>G (hg19) ; chr18:g.57550576C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550576C>G , CM000680.2:g.57550576C>G	GRCh38
NC_000018.9:g.55217808C>G , CM000680.1:g.55217808C>G	GRCh37
NC_000018.8:g.53368806C>G	NCBI36
NG_008175.1:g.41162G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.*136G>C MANE Select	ENSP00000262093.6:n.*136G>C
ENST00000382873.8:c.*136G>C	ENSP00000372326.4:n.*136G>C
ENST00000651787.1:n.1514G>C
ENST00000652755.1:c.*136G>C	ENSP00000498358.1:n.*136G>C
ENST00000262093.9:c.*136G>C	ENSP00000262093.5:n.*136G>C
ENST00000382873.7:c.*136G>C	ENSP00000372326.3:n.*136G>C
ENST00000585494.5:c.*1135G>C	ENSP00000465243.1:n.*1135G>C
NM_000140.3:c.*136G>C	NP_000131.2:n.*136G>C
NM_001012515.2:c.*136G>C	NP_001012533.1:n.*136G>C
XM_011525881.1:c.*136G>C	XP_011524183.1:n.*136G>C
XM_011525882.1:c.*136G>C	XP_011524184.1:n.*136G>C
NM_000140.4:c.*136G>C	NP_000131.2:n.*136G>C
NM_001012515.3:c.*136G>C	NP_001012533.1:n.*136G>C
XM_011525882.2:c.*136G>C	XP_011524184.1:n.*136G>C
XM_017025614.2:c.*136G>C	XP_016881103.1:n.*136G>C
NM_000140.5:c.*136G>C MANE Select	NP_000131.2:n.*136G>C
NM_001012515.4:c.*136G>C	NP_001012533.1:n.*136G>C
NM_001371094.1:c.*136G>C	NP_001358023.1:n.*136G>C
NM_001371095.1:c.*136G>C	NP_001358024.1:n.*136G>C
NM_001374778.1:c.*136G>C	NP_001361707.1:n.*136G>C