Canonical Allele Identifier: CA2530262469

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57554192_57554193insA , CM000680.2:g.57554192_57554193insA	GRCh38
NC_000018.9:g.55221424_55221425insA , CM000680.1:g.55221424_55221425insA	GRCh37
NC_000018.8:g.53372422_53372423insA	NCBI36
NG_008175.1:g.37545_37546insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682485.1:n.1319_1320insT
ENST00000262093.11:c.1077+67_1077+68insT MANE Select	ENSP00000262093.6:n.1077+67_1077+68insT
ENST00000382873.8:c.861+67_861+68insT	ENSP00000372326.4:n.861+67_861+68insT
ENST00000651787.1:n.1183+67_1183+68insT
ENST00000652755.1:c.1095+67_1095+68insT	ENSP00000498358.1:n.1095+67_1095+68insT
ENST00000262093.9:c.1077+67_1077+68insT	ENSP00000262093.5:n.1077+67_1077+68insT
ENST00000382873.7:c.1095+67_1095+68insT	ENSP00000372326.3:n.1095+67_1095+68insT
ENST00000585494.5:c.*804+67_*804+68insT	ENSP00000465243.1:n.*804+67_*804+68insT
ENST00000591977.5:c.344+67_344+68insT
NM_000140.3:c.1077+67_1077+68insT	NP_000131.2:n.1077+67_1077+68insT
NM_001012515.2:c.1095+67_1095+68insT	NP_001012533.1:n.1095+67_1095+68insT
XM_011525881.1:c.996+67_996+68insT	XP_011524183.1:n.996+67_996+68insT
XM_011525882.1:c.861+67_861+68insT	XP_011524184.1:n.861+67_861+68insT
NM_000140.4:c.1077+67_1077+68insT	NP_000131.2:n.1077+67_1077+68insT
NM_001012515.3:c.1095+67_1095+68insT	NP_001012533.1:n.1095+67_1095+68insT
XM_011525882.2:c.861+67_861+68insT	XP_011524184.1:n.861+67_861+68insT
XM_017025614.2:c.978+67_978+68insT	XP_016881103.1:n.978+67_978+68insT
NM_000140.5:c.1077+67_1077+68insT MANE Select	NP_000131.2:n.1077+67_1077+68insT
NM_001012515.4:c.1095+67_1095+68insT	NP_001012533.1:n.1095+67_1095+68insT
NM_001371094.1:c.978+67_978+68insT	NP_001358023.1:n.978+67_978+68insT
NM_001371095.1:c.861+67_861+68insT	NP_001358024.1:n.861+67_861+68insT
NM_001374778.1:c.1077+67_1077+68insT	NP_001361707.1:n.1077+67_1077+68insT