Canonical Allele Identifier: CA2306047541

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554703_57554705delinsCAG , CM000680.2:g.57554703_57554705delinsCAG	GRCh38
NC_000018.9:g.55221935_55221937delinsCAG , CM000680.1:g.55221935_55221937delinsCAG	GRCh37
NC_000018.8:g.53372933_53372935delinsCAG	NCBI36
NG_008175.1:g.37033_37035delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.813+140_813+142delinsCTG	ENSP00000466263.1:n.813+140_813+142delinsCTG
ENST00000682485.1:n.1087+140_1087+142delinsCTG
ENST00000262093.11:c.912+140_912+142delinsCTG MANE Select	ENSP00000262093.6:n.912+140_912+142delinsCTG
ENST00000382873.8:c.696+140_696+142delinsCTG	ENSP00000372326.4:n.696+140_696+142delinsCTG
ENST00000651787.1:n.1018+140_1018+142delinsCTG
ENST00000651812.1:n.509+140_509+142delinsCTG
ENST00000652755.1:c.930+140_930+142delinsCTG	ENSP00000498358.1:n.930+140_930+142delinsCTG
ENST00000262093.9:c.912+140_912+142delinsCTG	ENSP00000262093.5:n.912+140_912+142delinsCTG
ENST00000382873.7:c.930+140_930+142delinsCTG	ENSP00000372326.3:n.930+140_930+142delinsCTG
ENST00000585494.5:c.*639+140_*639+142delinsCTG	ENSP00000465243.1:n.*639+140_*639+142delinsCTG
ENST00000591977.5:c.179+140_179+142delinsCTG
ENST00000592699.5:c.813+140_813+142delinsCTG	ENSP00000466263.1:n.813+140_813+142delinsCTG
NM_000140.3:c.912+140_912+142delinsCTG	NP_000131.2:n.912+140_912+142delinsCTG
NM_001012515.2:c.930+140_930+142delinsCTG	NP_001012533.1:n.930+140_930+142delinsCTG
XM_011525881.1:c.831+140_831+142delinsCTG	XP_011524183.1:n.831+140_831+142delinsCTG
XM_011525882.1:c.696+140_696+142delinsCTG	XP_011524184.1:n.696+140_696+142delinsCTG
NM_000140.4:c.912+140_912+142delinsCTG	NP_000131.2:n.912+140_912+142delinsCTG
NM_001012515.3:c.930+140_930+142delinsCTG	NP_001012533.1:n.930+140_930+142delinsCTG
XM_011525882.2:c.696+140_696+142delinsCTG	XP_011524184.1:n.696+140_696+142delinsCTG
XM_017025614.2:c.813+140_813+142delinsCTG	XP_016881103.1:n.813+140_813+142delinsCTG
NM_000140.5:c.912+140_912+142delinsCTG MANE Select	NP_000131.2:n.912+140_912+142delinsCTG
NM_001012515.4:c.930+140_930+142delinsCTG	NP_001012533.1:n.930+140_930+142delinsCTG
NM_001371094.1:c.813+140_813+142delinsCTG	NP_001358023.1:n.813+140_813+142delinsCTG
NM_001371095.1:c.696+140_696+142delinsCTG	NP_001358024.1:n.696+140_696+142delinsCTG
NM_001374778.1:c.912+140_912+142delinsCTG	NP_001361707.1:n.912+140_912+142delinsCTG