Canonical Allele Identifier: CA1978652490

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64211663G= , CM000673.2:g.64211663G=	GRCh38
NC_000011.9:g.63979135G= , CM000673.1:g.63979135G=	GRCh37
NC_000011.8:g.63735711G=	NCBI36
NG_016360.1:g.9984G= , LRG_180:g.9984G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.702G=	ENSP00000279227.5:p.Arg234=
ENST00000541252.2:c.162G=	ENSP00000438885.2:p.Arg54=
ENST00000541326.6:n.19G=
ENST00000544997.6:c.702G=	ENSP00000445778.2:p.Arg234=
ENST00000546255.2:n.796G=
ENST00000698845.1:c.702G=	ENSP00000513981.1:p.Arg234=
ENST00000698846.1:n.839G=
ENST00000698847.1:c.*107G=	ENSP00000513982.1:n.*107G=
ENST00000698850.1:n.14G=
ENST00000698852.1:c.702G=	ENSP00000513984.1:p.Arg234=
ENST00000698853.1:c.702G=	ENSP00000513985.1:p.Arg234=
ENST00000698854.1:c.702G=	ENSP00000513986.1:p.Arg234=
ENST00000698855.1:n.2354G=
ENST00000698856.1:n.1622G=
ENST00000698859.1:n.866G=
ENST00000698860.1:c.702G=	ENSP00000513988.1:p.Arg234=
ENST00000698861.1:c.702G=	ENSP00000513989.1:p.Arg234=
ENST00000698862.1:c.702G=	ENSP00000513990.1:p.Arg234=
ENST00000698863.1:c.702G=	ENSP00000513991.1:p.Arg234=
ENST00000698864.1:n.808G=
ENST00000698865.1:c.702G=	ENSP00000513992.1:p.Arg234=
ENST00000698866.1:c.*107G=	ENSP00000513993.1:n.*107G=
ENST00000698867.1:n.4411G=
ENST00000698868.1:c.702G=	ENSP00000513994.1:p.Arg234=
ENST00000698869.1:c.702G=	ENSP00000513995.1:p.Arg234=
ENST00000698870.1:c.702G=	ENSP00000513996.1:p.Arg234=
ENST00000698871.1:n.959G=
ENST00000698872.1:c.162G=	ENSP00000513997.1:p.Arg54=
ENST00000698873.1:c.162G=	ENSP00000513998.1:p.Arg54=
ENST00000698874.1:c.162G=	ENSP00000513999.1:p.Arg54=
ENST00000698875.1:n.562G=
ENST00000698878.1:c.702G=	ENSP00000514000.1:p.Arg234=
ENST00000698879.1:c.611G=
ENST00000698880.1:c.542G=
ENST00000345728.10:c.702G= MANE Select	ENSP00000339950.5:p.Arg234=
ENST00000279227.9:c.702G=	ENSP00000279227.5:p.Arg234=
ENST00000345728.9:c.702G=	ENSP00000339950.5:p.Arg234=
ENST00000541252.1:c.162G=	ENSP00000438885.1:p.Arg54=
ENST00000541326.5:n.14G=
ENST00000544997.5:c.702G=	ENSP00000445778.1:p.Arg234=
NM_031471.5:c.702G=	NP_113659.3:p.Arg234=
NM_178443.2:c.702G= , LRG_180t1:c.702G=	NP_848537.1:p.Arg234=
XM_011545294.1:c.702G=	XP_011543596.1:p.Arg234=
XM_011545295.1:c.162G=	XP_011543597.1:p.Arg54=
XM_011545296.1:c.162G=	XP_011543598.1:p.Arg54=
XM_011545294.3:c.702G=	XP_011543596.1:p.Arg234=
XM_011545295.2:c.162G=	XP_011543597.1:p.Arg54=
XM_017018398.2:c.702G=	XP_016873887.1:p.Arg234=
XM_017018399.1:c.162G=	XP_016873888.1:p.Arg54=
NM_031471.6:c.702G= MANE Select	NP_113659.3:p.Arg234=
NM_001382361.1:c.702G=	NP_001369290.1:p.Arg234=
NM_001382362.1:c.702G=	NP_001369291.1:p.Arg234=
NM_001382363.1:c.162G=	NP_001369292.1:p.Arg54=
NM_001382364.1:c.162G=	NP_001369293.1:p.Arg54=
NM_001382448.1:c.702G=	NP_001369377.1:p.Arg234=
NM_178443.3:c.702G=	NP_848537.1:p.Arg234=