Canonical Allele Identifier: CA2641944342

Gene: FECH

Linked Data

• gnomAD v4: 18-57573504-A-ATGTCCCCGAATAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573505_57573506insGTCCCCGAATAGGT , CM000680.2:g.57573505_57573506insGTCCCCGAATAGGT	GRCh38
NC_000018.9:g.55240737_55240738insGTCCCCGAATAGGT , CM000680.1:g.55240737_55240738insGTCCCCGAATAGGT	GRCh37
NC_000018.8:g.53391735_53391736insGTCCCCGAATAGGT	NCBI36
NG_008175.1:g.18233_18234insCCTATTCGGGGACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.195-140_195-139insCCTATTCGGGGACA	ENSP00000466263.1:n.195-140_195-139insCCTATTCGGGGACA
ENST00000682485.1:n.307-140_307-139insCCTATTCGGGGACA
ENST00000262093.11:c.195-140_195-139insCCTATTCGGGGACA MANE Select	ENSP00000262093.6:n.195-140_195-139insCCTATTCGGGGACA
ENST00000382873.8:c.-22-140_-22-139insCCTATTCGGGGACA	ENSP00000372326.4:n.-22-140_-22-139insCCTATTCGGGGACA
ENST00000651787.1:n.301-140_301-139insCCTATTCGGGGACA
ENST00000652755.1:c.213-140_213-139insCCTATTCGGGGACA	ENSP00000498358.1:n.213-140_213-139insCCTATTCGGGGACA
ENST00000262093.9:c.195-140_195-139insCCTATTCGGGGACA	ENSP00000262093.5:n.195-140_195-139insCCTATTCGGGGACA
ENST00000382873.7:c.213-140_213-139insCCTATTCGGGGACA	ENSP00000372326.3:n.213-140_213-139insCCTATTCGGGGACA
ENST00000585494.5:c.195-140_195-139insCCTATTCGGGGACA	ENSP00000465243.1:n.195-140_195-139insCCTATTCGGGGACA
ENST00000585699.1:n.147-140_147-139insCCTATTCGGGGACA
ENST00000585747.1:c.195-140_195-139insCCTATTCGGGGACA	ENSP00000465717.1:n.195-140_195-139insCCTATTCGGGGACA
ENST00000585878.1:n.247-140_247-139insCCTATTCGGGGACA
ENST00000591215.5:c.-22-140_-22-139insCCTATTCGGGGACA	ENSP00000467461.1:n.-22-140_-22-139insCCTATTCGGGGACA
ENST00000592111.1:n.196-140_196-139insCCTATTCGGGGACA
ENST00000592699.5:c.195-140_195-139insCCTATTCGGGGACA	ENSP00000466263.1:n.195-140_195-139insCCTATTCGGGGACA
NM_000140.3:c.195-140_195-139insCCTATTCGGGGACA	NP_000131.2:n.195-140_195-139insCCTATTCGGGGACA
NM_001012515.2:c.213-140_213-139insCCTATTCGGGGACA	NP_001012533.1:n.213-140_213-139insCCTATTCGGGGACA
XM_011525881.1:c.213-140_213-139insCCTATTCGGGGACA	XP_011524183.1:n.213-140_213-139insCCTATTCGGGGACA
XM_011525882.1:c.-22-140_-22-139insCCTATTCGGGGACA	XP_011524184.1:n.-22-140_-22-139insCCTATTCGGGGACA
NM_000140.4:c.195-140_195-139insCCTATTCGGGGACA	NP_000131.2:n.195-140_195-139insCCTATTCGGGGACA
NM_001012515.3:c.213-140_213-139insCCTATTCGGGGACA	NP_001012533.1:n.213-140_213-139insCCTATTCGGGGACA
XM_011525882.2:c.-22-140_-22-139insCCTATTCGGGGACA	XP_011524184.1:n.-22-140_-22-139insCCTATTCGGGGACA
XM_017025614.2:c.195-140_195-139insCCTATTCGGGGACA	XP_016881103.1:n.195-140_195-139insCCTATTCGGGGACA
NM_000140.5:c.195-140_195-139insCCTATTCGGGGACA MANE Select	NP_000131.2:n.195-140_195-139insCCTATTCGGGGACA
NM_001012515.4:c.213-140_213-139insCCTATTCGGGGACA	NP_001012533.1:n.213-140_213-139insCCTATTCGGGGACA
NM_001371094.1:c.195-140_195-139insCCTATTCGGGGACA	NP_001358023.1:n.195-140_195-139insCCTATTCGGGGACA
NM_001371095.1:c.-22-140_-22-139insCCTATTCGGGGACA	NP_001358024.1:n.-22-140_-22-139insCCTATTCGGGGACA
NM_001374778.1:c.195-140_195-139insCCTATTCGGGGACA	NP_001361707.1:n.195-140_195-139insCCTATTCGGGGACA