Canonical Allele Identifier: CA10651904

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57549424_57549425insTAAA , CM000680.2:g.57549424_57549425insTAAA	GRCh38
NC_000018.9:g.55216656_55216657insTAAA , CM000680.1:g.55216656_55216657insTAAA	GRCh37
NC_000018.8:g.53367654_53367655insTAAA	NCBI36
NG_008175.1:g.42313_42314insTTTA

Transcript Alleles

HGVS	Amino-acid Change
NM_000140.5:c.*1287_*1288insTTTA MANE Select	NP_000131.2:n.*1287_*1288insTTTA
ENST00000262093.11:c.*1287_*1288insTTTA MANE Select	ENSP00000262093.6:n.*1287_*1288insTTTA
NM_000140.3:c.*1287_*1288insTTTA	NP_000131.2:n.*1287_*1288insTTTA
NM_000140.4:c.*1287_*1288insTTTA	NP_000131.2:n.*1287_*1288insTTTA
NM_001012515.2:c.*1287_*1288insTTTA	NP_001012533.1:n.*1287_*1288insTTTA
NM_001012515.3:c.*1287_*1288insTTTA	NP_001012533.1:n.*1287_*1288insTTTA
NM_001012515.4:c.*1287_*1288insTTTA	NP_001012533.1:n.*1287_*1288insTTTA
NM_001371094.1:c.*1287_*1288insTTTA	NP_001358023.1:n.*1287_*1288insTTTA
NM_001371095.1:c.*1287_*1288insTTTA	NP_001358024.1:n.*1287_*1288insTTTA
NM_001374778.1:c.*1287_*1288insTTTA	NP_001361707.1:n.*1287_*1288insTTTA
ENST00000262093.9:c.*1287_*1288insTTTA	ENSP00000262093.5:n.*1287_*1288insTTTA
ENST00000652755.1:c.*1287_*1288insTTTA	ENSP00000498358.1:n.*1287_*1288insTTTA
XM_011525881.1:c.*1287_*1288insTTTA	XP_011524183.1:n.*1287_*1288insTTTA
XM_011525882.1:c.*1287_*1288insTTTA	XP_011524184.1:n.*1287_*1288insTTTA
XM_011525882.2:c.*1287_*1288insTTTA	XP_011524184.1:n.*1287_*1288insTTTA