Canonical Allele Identifier: CA2641944239

Gene: FECH

Linked Data

• gnomAD v4: 18-57573155-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573155A>G , CM000680.2:g.57573155A>G	GRCh38
NC_000018.9:g.55240387A>G , CM000680.1:g.55240387A>G	GRCh37
NC_000018.8:g.53391385A>G	NCBI36
NG_008175.1:g.18583T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.314+91T>C	ENSP00000466263.1:n.314+91T>C
ENST00000682485.1:n.426+91T>C
ENST00000262093.11:c.314+91T>C MANE Select	ENSP00000262093.6:n.314+91T>C
ENST00000382873.8:c.98+91T>C	ENSP00000372326.4:n.98+91T>C
ENST00000651787.1:n.420+91T>C
ENST00000652755.1:c.332+91T>C	ENSP00000498358.1:n.332+91T>C
ENST00000262093.9:c.314+91T>C	ENSP00000262093.5:n.314+91T>C
ENST00000382873.7:c.332+91T>C	ENSP00000372326.3:n.332+91T>C
ENST00000585494.5:c.314+91T>C	ENSP00000465243.1:n.314+91T>C
ENST00000585699.1:n.266+91T>C
ENST00000585747.1:c.314+91T>C	ENSP00000465717.1:n.314+91T>C
ENST00000585878.1:n.457T>C
ENST00000591215.5:c.98+91T>C	ENSP00000467461.1:n.98+91T>C
ENST00000592111.1:n.406T>C
ENST00000592699.5:c.314+91T>C	ENSP00000466263.1:n.314+91T>C
NM_000140.3:c.314+91T>C	NP_000131.2:n.314+91T>C
NM_001012515.2:c.332+91T>C	NP_001012533.1:n.332+91T>C
XM_011525881.1:c.332+91T>C	XP_011524183.1:n.332+91T>C
XM_011525882.1:c.98+91T>C	XP_011524184.1:n.98+91T>C
NM_000140.4:c.314+91T>C	NP_000131.2:n.314+91T>C
NM_001012515.3:c.332+91T>C	NP_001012533.1:n.332+91T>C
XM_011525882.2:c.98+91T>C	XP_011524184.1:n.98+91T>C
XM_017025614.2:c.314+91T>C	XP_016881103.1:n.314+91T>C
NM_000140.5:c.314+91T>C MANE Select	NP_000131.2:n.314+91T>C
NM_001012515.4:c.332+91T>C	NP_001012533.1:n.332+91T>C
NM_001371094.1:c.314+91T>C	NP_001358023.1:n.314+91T>C
NM_001371095.1:c.98+91T>C	NP_001358024.1:n.98+91T>C
NM_001374778.1:c.314+91T>C	NP_001361707.1:n.314+91T>C