Canonical Allele Identifier: CA1504935635

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569773_154569774delinsCA , CM000666.2:g.154569773_154569774delinsCA	GRCh38
NC_000004.11:g.155490925_155490926delinsCA , CM000666.1:g.155490925_155490926delinsCA	GRCh37
NC_000004.10:g.155710375_155710376delinsCA	NCBI36
NG_008833.1:g.11794_11795delinsCA , LRG_558:g.11794_11795delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1218_1219delinsCA MANE Select	ENSP00000306099.4:p.Ser406=
ENST00000302068.8:c.1218_1219delinsCA	ENSP00000306099.4:p.Ser406=
ENST00000502545.5:n.939+466_939+467delinsCA
ENST00000509493.1:c.561_562delinsCA	ENSP00000426757.1:p.Ser187=
NM_001184741.1:c.1041_1042delinsCA	NP_001171670.1:p.Ser347=
NM_005141.4:c.1218_1219delinsCA , LRG_558t1:c.1218_1219delinsCA	NP_005132.2:p.Ser406=
NM_001382759.1:c.1086_1087delinsCA	NP_001369688.1:p.Ser362=
NM_001382760.1:c.1218_1219delinsCA	NP_001369689.1:p.Ser406=
NM_001382761.1:c.1218_1219delinsCA	NP_001369690.1:p.Ser406=
NM_001382762.1:c.918_919delinsCA	NP_001369691.1:p.Ser306=
NM_001382763.1:c.1209_1210delinsCA	NP_001369692.1:p.Ser403=
NM_001382764.1:c.1081_1082delinsCA	NP_001369693.1:p.His361=
NM_001382765.1:c.1218_1219delinsCA	NP_001369694.1:p.Ser406=
NM_005141.5:c.1218_1219delinsCA MANE Select	NP_005132.2:p.Ser406=