Canonical Allele Identifier: CA475151823

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990610C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223138C>A , CM000673.2:g.64223138C>A	GRCh38
NC_000011.9:g.63990610C>A , CM000673.1:g.63990610C>A	GRCh37
NC_000011.8:g.63747186C>A	NCBI36
NG_016360.1:g.21459C>A , LRG_180:g.21459C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1773C>A	ENSP00000279227.5:p.Thr591=
ENST00000540554.2:n.3285C>A
ENST00000541252.2:c.1221C>A	ENSP00000438885.2:p.Thr407=
ENST00000544997.6:c.1761C>A	ENSP00000445778.2:p.Thr587=
ENST00000545896.2:c.325C>A	ENSP00000440209.2:p.Leu109Met
ENST00000546255.2:n.2065C>A
ENST00000698845.1:c.*956C>A	ENSP00000513981.1:n.*956C>A
ENST00000698846.1:n.2007C>A
ENST00000698847.1:c.*1166C>A	ENSP00000513982.1:n.*1166C>A
ENST00000698850.1:n.3782C>A
ENST00000698852.1:c.1761C>A	ENSP00000513984.1:p.Thr587=
ENST00000698853.1:c.*990C>A	ENSP00000513985.1:n.*990C>A
ENST00000698854.1:c.*1091C>A	ENSP00000513986.1:n.*1091C>A
ENST00000698855.1:n.3413C>A
ENST00000698856.1:n.3107C>A
ENST00000698859.1:n.2271C>A
ENST00000698860.1:c.1773C>A	ENSP00000513988.1:p.Thr591=
ENST00000698861.1:c.1761C>A	ENSP00000513989.1:p.Thr587=
ENST00000698862.1:c.*1057C>A	ENSP00000513990.1:n.*1057C>A
ENST00000698863.1:c.1761C>A	ENSP00000513991.1:p.Thr587=
ENST00000698864.1:n.2322C>A
ENST00000698865.1:c.1782C>A	ENSP00000513992.1:p.Thr594=
ENST00000698866.1:c.*1549C>A	ENSP00000513993.1:n.*1549C>A
ENST00000698867.1:n.5736C>A
ENST00000698868.1:c.1626C>A	ENSP00000513994.1:p.Thr542=
ENST00000698869.1:c.1527C>A	ENSP00000513995.1:p.Thr509=
ENST00000698870.1:c.1761C>A	ENSP00000513996.1:p.Thr587=
ENST00000698871.1:n.2284C>A
ENST00000698872.1:c.*550C>A	ENSP00000513997.1:n.*550C>A
ENST00000698873.1:c.*956C>A	ENSP00000513998.1:n.*956C>A
ENST00000698874.1:c.1221C>A	ENSP00000513999.1:p.Thr407=
ENST00000698875.1:n.1621C>A
ENST00000698876.1:n.1809C>A
ENST00000698877.1:n.1329C>A
ENST00000698878.1:c.1755C>A	ENSP00000514000.1:p.Thr585=
ENST00000698880.1:c.1629C>A
ENST00000345728.10:c.1761C>A MANE Select	ENSP00000339950.5:p.Thr587=
ENST00000279227.9:c.1773C>A	ENSP00000279227.5:p.Thr591=
ENST00000345728.9:c.1761C>A	ENSP00000339950.5:p.Thr587=
ENST00000545896.1:c.324C>A	ENSP00000440209.1:p.Thr108=
NM_031471.5:c.1761C>A	NP_113659.3:p.Thr587=
NM_178443.2:c.1773C>A , LRG_180t1:c.1773C>A	NP_848537.1:p.Thr591=
XM_011545294.1:c.1773C>A	XP_011543596.1:p.Thr591=
XM_011545295.1:c.1233C>A	XP_011543597.1:p.Thr411=
XM_011545296.1:c.1233C>A	XP_011543598.1:p.Thr411=
XM_011545294.3:c.1773C>A	XP_011543596.1:p.Thr591=
XM_011545295.2:c.1233C>A	XP_011543597.1:p.Thr411=
XM_017018398.2:c.1761C>A	XP_016873887.1:p.Thr587=
XM_017018399.1:c.1221C>A	XP_016873888.1:p.Thr407=
NM_031471.6:c.1761C>A MANE Select	NP_113659.3:p.Thr587=
NM_001382361.1:c.1761C>A	NP_001369290.1:p.Thr587=
NM_001382362.1:c.1773C>A	NP_001369291.1:p.Thr591=
NM_001382363.1:c.1221C>A	NP_001369292.1:p.Thr407=
NM_001382364.1:c.1233C>A	NP_001369293.1:p.Thr411=
NM_001382448.1:c.1761C>A	NP_001369377.1:p.Thr587=
NM_178443.3:c.1773C>A	NP_848537.1:p.Thr591=