Canonical Allele Identifier: CA1978642784

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223079G= , CM000673.2:g.64223079G=	GRCh38
NC_000011.9:g.63990551G= , CM000673.1:g.63990551G=	GRCh37
NC_000011.8:g.63747127G=	NCBI36
NG_016360.1:g.21400G= , LRG_180:g.21400G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1714G=	ENSP00000279227.5:p.Gly572=
ENST00000540554.2:n.3226G=
ENST00000541252.2:c.1162G=	ENSP00000438885.2:p.Gly388=
ENST00000544997.6:c.1702G=	ENSP00000445778.2:p.Gly568=
ENST00000545896.2:c.266G=	ENSP00000440209.2:p.Gly89=
ENST00000546255.2:n.2006G=
ENST00000698845.1:c.*897G=	ENSP00000513981.1:n.*897G=
ENST00000698846.1:n.1948G=
ENST00000698847.1:c.*1107G=	ENSP00000513982.1:n.*1107G=
ENST00000698850.1:n.3723G=
ENST00000698852.1:c.1702G=	ENSP00000513984.1:p.Gly568=
ENST00000698853.1:c.*931G=	ENSP00000513985.1:n.*931G=
ENST00000698854.1:c.*1032G=	ENSP00000513986.1:n.*1032G=
ENST00000698855.1:n.3354G=
ENST00000698856.1:n.3048G=
ENST00000698859.1:n.2212G=
ENST00000698860.1:c.1714G=	ENSP00000513988.1:p.Gly572=
ENST00000698861.1:c.1702G=	ENSP00000513989.1:p.Gly568=
ENST00000698862.1:c.*998G=	ENSP00000513990.1:n.*998G=
ENST00000698863.1:c.1702G=	ENSP00000513991.1:p.Gly568=
ENST00000698864.1:n.2263G=
ENST00000698865.1:c.1723G=	ENSP00000513992.1:p.Gly575=
ENST00000698866.1:c.*1490G=	ENSP00000513993.1:n.*1490G=
ENST00000698867.1:n.5677G=
ENST00000698868.1:c.1567G=	ENSP00000513994.1:p.Gly523=
ENST00000698869.1:c.1468G=	ENSP00000513995.1:p.Gly490=
ENST00000698870.1:c.1702G=	ENSP00000513996.1:p.Gly568=
ENST00000698871.1:n.2225G=
ENST00000698872.1:c.*491G=	ENSP00000513997.1:n.*491G=
ENST00000698873.1:c.*897G=	ENSP00000513998.1:n.*897G=
ENST00000698874.1:c.1162G=	ENSP00000513999.1:p.Gly388=
ENST00000698875.1:n.1562G=
ENST00000698876.1:n.1750G=
ENST00000698877.1:n.1270G=
ENST00000698878.1:c.1696G=	ENSP00000514000.1:p.Gly566=
ENST00000698880.1:c.1570G=
ENST00000345728.10:c.1702G= MANE Select	ENSP00000339950.5:p.Gly568=
ENST00000279227.9:c.1714G=	ENSP00000279227.5:p.Gly572=
ENST00000345728.9:c.1702G=	ENSP00000339950.5:p.Gly568=
ENST00000540554.1:n.338G=
ENST00000545896.1:c.265G=	ENSP00000440209.1:p.Gly89=
NM_031471.5:c.1702G=	NP_113659.3:p.Gly568=
NM_178443.2:c.1714G= , LRG_180t1:c.1714G=	NP_848537.1:p.Gly572=
XM_011545294.1:c.1714G=	XP_011543596.1:p.Gly572=
XM_011545295.1:c.1174G=	XP_011543597.1:p.Gly392=
XM_011545296.1:c.1174G=	XP_011543598.1:p.Gly392=
XM_011545294.3:c.1714G=	XP_011543596.1:p.Gly572=
XM_011545295.2:c.1174G=	XP_011543597.1:p.Gly392=
XM_017018398.2:c.1702G=	XP_016873887.1:p.Gly568=
XM_017018399.1:c.1162G=	XP_016873888.1:p.Gly388=
NM_031471.6:c.1702G= MANE Select	NP_113659.3:p.Gly568=
NM_001382361.1:c.1702G=	NP_001369290.1:p.Gly568=
NM_001382362.1:c.1714G=	NP_001369291.1:p.Gly572=
NM_001382363.1:c.1162G=	NP_001369292.1:p.Gly388=
NM_001382364.1:c.1174G=	NP_001369293.1:p.Gly392=
NM_001382448.1:c.1702G=	NP_001369377.1:p.Gly568=
NM_178443.3:c.1714G=	NP_848537.1:p.Gly572=