Canonical Allele Identifier: CA10641801

Gene: FECH

Linked Data

• ClinVar Variation Id: 327377
• ClinVar RCV Id: RCV000308269
• dbSNP Id: rs1555678907
• MyVariant Identifiers: chr18:g.55215492_55215493insC (hg19) ; chr18:g.57548260_57548261insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57548260_57548261insC , CM000680.2:g.57548260_57548261insC	GRCh38
NC_000018.9:g.55215492_55215493insC , CM000680.1:g.55215492_55215493insC	GRCh37
NC_000018.8:g.53366490_53366491insC	NCBI36
NG_008175.1:g.43477_43478insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.*2451_*2452insG MANE Select	ENSP00000262093.6:n.*2451_*2452insG
ENST00000652755.1:c.*2451_*2452insG	ENSP00000498358.1:n.*2451_*2452insG
NM_000140.3:c.*2451_*2452insG	NP_000131.2:n.*2451_*2452insG
NM_001012515.2:c.*2451_*2452insG	NP_001012533.1:n.*2451_*2452insG
NM_000140.4:c.*2451_*2452insG	NP_000131.2:n.*2451_*2452insG
NM_001012515.3:c.*2451_*2452insG	NP_001012533.1:n.*2451_*2452insG
NM_000140.5:c.*2451_*2452insG MANE Select	NP_000131.2:n.*2451_*2452insG
NM_001012515.4:c.*2451_*2452insG	NP_001012533.1:n.*2451_*2452insG
NM_001371094.1:c.*2451_*2452insG	NP_001358023.1:n.*2451_*2452insG
NM_001371095.1:c.*2451_*2452insG	NP_001358024.1:n.*2451_*2452insG
NM_001374778.1:c.*2451_*2452insG	NP_001361707.1:n.*2451_*2452insG