Canonical Allele Identifier: CA402541449

Gene: FECH

Linked Data

• gnomAD v4: 18-57554929-A-C
• MyVariant Identifiers: chr18:g.55222161A>C (hg19) ; chr18:g.57554929A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554929A>C , CM000680.2:g.57554929A>C	GRCh38
NC_000018.9:g.55222161A>C , CM000680.1:g.55222161A>C	GRCh37
NC_000018.8:g.53373159A>C	NCBI36
NG_008175.1:g.36809T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.729T>G	ENSP00000466263.1:p.Tyr243Ter
ENST00000682485.1:n.1003T>G
ENST00000262093.11:c.828T>G MANE Select	ENSP00000262093.6:p.Tyr276Ter
ENST00000382873.8:c.612T>G	ENSP00000372326.4:p.Tyr204Ter
ENST00000651787.1:n.934T>G
ENST00000651812.1:n.425T>G
ENST00000652755.1:c.846T>G	ENSP00000498358.1:p.Tyr282Ter
ENST00000262093.9:c.828T>G	ENSP00000262093.5:p.Tyr276Ter
ENST00000382873.7:c.846T>G	ENSP00000372326.3:p.Tyr282Ter
ENST00000585494.5:c.*555T>G	ENSP00000465243.1:n.*555T>G
ENST00000591977.5:c.95T>G
ENST00000592699.5:c.729T>G	ENSP00000466263.1:p.Tyr243Ter
NM_000140.3:c.828T>G	NP_000131.2:p.Tyr276Ter
NM_001012515.2:c.846T>G	NP_001012533.1:p.Tyr282Ter
XM_011525881.1:c.747T>G	XP_011524183.1:p.Tyr249Ter
XM_011525882.1:c.612T>G	XP_011524184.1:p.Tyr204Ter
NM_000140.4:c.828T>G	NP_000131.2:p.Tyr276Ter
NM_001012515.3:c.846T>G	NP_001012533.1:p.Tyr282Ter
XM_011525882.2:c.612T>G	XP_011524184.1:p.Tyr204Ter
XM_017025614.2:c.729T>G	XP_016881103.1:p.Tyr243Ter
NM_000140.5:c.828T>G MANE Select	NP_000131.2:p.Tyr276Ter
NM_001012515.4:c.846T>G	NP_001012533.1:p.Tyr282Ter
NM_001371094.1:c.729T>G	NP_001358023.1:p.Tyr243Ter
NM_001371095.1:c.612T>G	NP_001358024.1:p.Tyr204Ter
NM_001374778.1:c.828T>G	NP_001361707.1:p.Tyr276Ter