Canonical Allele Identifier: CA1978643027

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223191T= , CM000673.2:g.64223191T=	GRCh38
NC_000011.9:g.63990663T= , CM000673.1:g.63990663T=	GRCh37
NC_000011.8:g.63747239T=	NCBI36
NG_016360.1:g.21512T= , LRG_180:g.21512T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1824+2T=	ENSP00000279227.5:n.1824+2T=
ENST00000540554.2:n.3336+2T=
ENST00000541252.2:c.1272+2T=	ENSP00000438885.2:n.1272+2T=
ENST00000544997.6:c.1812+2T=	ENSP00000445778.2:n.1812+2T=
ENST00000545896.2:c.376+2T=	ENSP00000440209.2:n.376+2T=
ENST00000546255.2:n.2116+2T=
ENST00000698845.1:c.*1007+2T=	ENSP00000513981.1:n.*1007+2T=
ENST00000698846.1:n.2058+2T=
ENST00000698847.1:c.*1217+2T=	ENSP00000513982.1:n.*1217+2T=
ENST00000698850.1:n.3833+2T=
ENST00000698852.1:c.1812+2T=	ENSP00000513984.1:n.1812+2T=
ENST00000698853.1:c.*1041+2T=	ENSP00000513985.1:n.*1041+2T=
ENST00000698854.1:c.*1142+2T=	ENSP00000513986.1:n.*1142+2T=
ENST00000698855.1:n.3464+2T=
ENST00000698856.1:n.3158+2T=
ENST00000698859.1:n.2322+2T=
ENST00000698860.1:c.1824+2T=	ENSP00000513988.1:n.1824+2T=
ENST00000698861.1:c.1812+2T=	ENSP00000513989.1:n.1812+2T=
ENST00000698862.1:c.*1108+2T=	ENSP00000513990.1:n.*1108+2T=
ENST00000698863.1:c.1812+2T=	ENSP00000513991.1:n.1812+2T=
ENST00000698864.1:n.2373+2T=
ENST00000698865.1:c.1833+2T=	ENSP00000513992.1:n.1833+2T=
ENST00000698866.1:c.*1600+2T=	ENSP00000513993.1:n.*1600+2T=
ENST00000698867.1:n.5787+2T=
ENST00000698868.1:c.1677+2T=	ENSP00000513994.1:n.1677+2T=
ENST00000698869.1:c.1578+2T=	ENSP00000513995.1:n.1578+2T=
ENST00000698870.1:c.1812+2T=	ENSP00000513996.1:n.1812+2T=
ENST00000698871.1:n.2335+2T=
ENST00000698872.1:c.*601+2T=	ENSP00000513997.1:n.*601+2T=
ENST00000698873.1:c.*1007+2T=	ENSP00000513998.1:n.*1007+2T=
ENST00000698874.1:c.1272+2T=	ENSP00000513999.1:n.1272+2T=
ENST00000698875.1:n.1672+2T=
ENST00000698876.1:n.1860+2T=
ENST00000698877.1:n.1380+2T=
ENST00000698878.1:c.1806+2T=	ENSP00000514000.1:n.1806+2T=
ENST00000698880.1:c.1680+2T=
ENST00000345728.10:c.1812+2T= MANE Select	ENSP00000339950.5:n.1812+2T=
ENST00000279227.9:c.1824+2T=	ENSP00000279227.5:n.1824+2T=
ENST00000345728.9:c.1812+2T=	ENSP00000339950.5:n.1812+2T=
ENST00000545896.1:c.375+2T=	ENSP00000440209.1:n.375+2T=
NM_031471.5:c.1812+2T=	NP_113659.3:n.1812+2T=
NM_178443.2:c.1824+2T= , LRG_180t1:c.1824+2T=	NP_848537.1:n.1824+2T=
XM_011545294.1:c.1824+2T=	XP_011543596.1:n.1824+2T=
XM_011545295.1:c.1284+2T=	XP_011543597.1:n.1284+2T=
XM_011545296.1:c.1284+2T=	XP_011543598.1:n.1284+2T=
XM_011545294.3:c.1824+2T=	XP_011543596.1:n.1824+2T=
XM_011545295.2:c.1284+2T=	XP_011543597.1:n.1284+2T=
XM_017018398.2:c.1812+2T=	XP_016873887.1:n.1812+2T=
XM_017018399.1:c.1272+2T=	XP_016873888.1:n.1272+2T=
NM_031471.6:c.1812+2T= MANE Select	NP_113659.3:n.1812+2T=
NM_001382361.1:c.1812+2T=	NP_001369290.1:n.1812+2T=
NM_001382362.1:c.1824+2T=	NP_001369291.1:n.1824+2T=
NM_001382363.1:c.1272+2T=	NP_001369292.1:n.1272+2T=
NM_001382364.1:c.1284+2T=	NP_001369293.1:n.1284+2T=
NM_001382448.1:c.1812+2T=	NP_001369377.1:n.1812+2T=
NM_178443.3:c.1824+2T=	NP_848537.1:n.1824+2T=