Canonical Allele Identifier: CA2306045886

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550612_57550621delinsGGATGACTTC , CM000680.2:g.57550612_57550621delinsGGATGACTTC	GRCh38
NC_000018.9:g.55217844_55217853delinsGGATGACTTC , CM000680.1:g.55217844_55217853delinsGGATGACTTC	GRCh37
NC_000018.8:g.53368842_53368851delinsGGATGACTTC	NCBI36
NG_008175.1:g.41117_41126delinsGAAGTCATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.*91_*100delinsGAAGTCATCC MANE Select	ENSP00000262093.6:n.*91_*100delinsGAAGTCATCC
ENST00000382873.8:c.*91_*100delinsGAAGTCATCC	ENSP00000372326.4:n.*91_*100delinsGAAGTCATCC
ENST00000651787.1:n.1469_1478delinsGAAGTCATCC
ENST00000652755.1:c.*91_*100delinsGAAGTCATCC	ENSP00000498358.1:n.*91_*100delinsGAAGTCATCC
ENST00000262093.9:c.*91_*100delinsGAAGTCATCC	ENSP00000262093.5:n.*91_*100delinsGAAGTCATCC
ENST00000382873.7:c.*91_*100delinsGAAGTCATCC	ENSP00000372326.3:n.*91_*100delinsGAAGTCATCC
ENST00000585494.5:c.*1090_*1099delinsGAAGTCATCC	ENSP00000465243.1:n.*1090_*1099delinsGAAGTCATCC
NM_000140.3:c.*91_*100delinsGAAGTCATCC	NP_000131.2:n.*91_*100delinsGAAGTCATCC
NM_001012515.2:c.*91_*100delinsGAAGTCATCC	NP_001012533.1:n.*91_*100delinsGAAGTCATCC
XM_011525881.1:c.*91_*100delinsGAAGTCATCC	XP_011524183.1:n.*91_*100delinsGAAGTCATCC
XM_011525882.1:c.*91_*100delinsGAAGTCATCC	XP_011524184.1:n.*91_*100delinsGAAGTCATCC
NM_000140.4:c.*91_*100delinsGAAGTCATCC	NP_000131.2:n.*91_*100delinsGAAGTCATCC
NM_001012515.3:c.*91_*100delinsGAAGTCATCC	NP_001012533.1:n.*91_*100delinsGAAGTCATCC
XM_011525882.2:c.*91_*100delinsGAAGTCATCC	XP_011524184.1:n.*91_*100delinsGAAGTCATCC
XM_017025614.2:c.*91_*100delinsGAAGTCATCC	XP_016881103.1:n.*91_*100delinsGAAGTCATCC
NM_000140.5:c.*91_*100delinsGAAGTCATCC MANE Select	NP_000131.2:n.*91_*100delinsGAAGTCATCC
NM_001012515.4:c.*91_*100delinsGAAGTCATCC	NP_001012533.1:n.*91_*100delinsGAAGTCATCC
NM_001371094.1:c.*91_*100delinsGAAGTCATCC	NP_001358023.1:n.*91_*100delinsGAAGTCATCC
NM_001371095.1:c.*91_*100delinsGAAGTCATCC	NP_001358024.1:n.*91_*100delinsGAAGTCATCC
NM_001374778.1:c.*91_*100delinsGAAGTCATCC	NP_001361707.1:n.*91_*100delinsGAAGTCATCC