Canonical Allele Identifier: CA475151760

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990532C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223060C>T , CM000673.2:g.64223060C>T	GRCh38
NC_000011.9:g.63990532C>T , CM000673.1:g.63990532C>T	GRCh37
NC_000011.8:g.63747108C>T	NCBI36
NG_016360.1:g.21381C>T , LRG_180:g.21381C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1695C>T	ENSP00000279227.5:p.Ser565=
ENST00000540554.2:n.3207C>T
ENST00000541252.2:c.1143C>T	ENSP00000438885.2:p.Ser381=
ENST00000544997.6:c.1683C>T	ENSP00000445778.2:p.Ser561=
ENST00000545896.2:c.247C>T	ENSP00000440209.2:p.Gln83Ter
ENST00000546255.2:n.1987C>T
ENST00000698845.1:c.*878C>T	ENSP00000513981.1:n.*878C>T
ENST00000698846.1:n.1929C>T
ENST00000698847.1:c.*1088C>T	ENSP00000513982.1:n.*1088C>T
ENST00000698850.1:n.3704C>T
ENST00000698852.1:c.1683C>T	ENSP00000513984.1:p.Ser561=
ENST00000698853.1:c.*912C>T	ENSP00000513985.1:n.*912C>T
ENST00000698854.1:c.*1013C>T	ENSP00000513986.1:n.*1013C>T
ENST00000698855.1:n.3335C>T
ENST00000698856.1:n.3029C>T
ENST00000698859.1:n.2193C>T
ENST00000698860.1:c.1695C>T	ENSP00000513988.1:p.Ser565=
ENST00000698861.1:c.1683C>T	ENSP00000513989.1:p.Ser561=
ENST00000698862.1:c.*979C>T	ENSP00000513990.1:n.*979C>T
ENST00000698863.1:c.1683C>T	ENSP00000513991.1:p.Ser561=
ENST00000698864.1:n.2244C>T
ENST00000698865.1:c.1704C>T	ENSP00000513992.1:p.Ser568=
ENST00000698866.1:c.*1471C>T	ENSP00000513993.1:n.*1471C>T
ENST00000698867.1:n.5658C>T
ENST00000698868.1:c.1548C>T	ENSP00000513994.1:p.Ser516=
ENST00000698869.1:c.1449C>T	ENSP00000513995.1:p.Ser483=
ENST00000698870.1:c.1683C>T	ENSP00000513996.1:p.Ser561=
ENST00000698871.1:n.2206C>T
ENST00000698872.1:c.*472C>T	ENSP00000513997.1:n.*472C>T
ENST00000698873.1:c.*878C>T	ENSP00000513998.1:n.*878C>T
ENST00000698874.1:c.1143C>T	ENSP00000513999.1:p.Ser381=
ENST00000698875.1:n.1543C>T
ENST00000698876.1:n.1731C>T
ENST00000698877.1:n.1251C>T
ENST00000698878.1:c.1677C>T	ENSP00000514000.1:p.Ser559=
ENST00000698880.1:c.1551C>T
ENST00000345728.10:c.1683C>T MANE Select	ENSP00000339950.5:p.Ser561=
ENST00000279227.9:c.1695C>T	ENSP00000279227.5:p.Ser565=
ENST00000345728.9:c.1683C>T	ENSP00000339950.5:p.Ser561=
ENST00000540554.1:n.319C>T
ENST00000545896.1:c.246C>T	ENSP00000440209.1:p.Ser82=
NM_031471.5:c.1683C>T	NP_113659.3:p.Ser561=
NM_178443.2:c.1695C>T , LRG_180t1:c.1695C>T	NP_848537.1:p.Ser565=
XM_011545294.1:c.1695C>T	XP_011543596.1:p.Ser565=
XM_011545295.1:c.1155C>T	XP_011543597.1:p.Ser385=
XM_011545296.1:c.1155C>T	XP_011543598.1:p.Ser385=
XM_011545294.3:c.1695C>T	XP_011543596.1:p.Ser565=
XM_011545295.2:c.1155C>T	XP_011543597.1:p.Ser385=
XM_017018398.2:c.1683C>T	XP_016873887.1:p.Ser561=
XM_017018399.1:c.1143C>T	XP_016873888.1:p.Ser381=
NM_031471.6:c.1683C>T MANE Select	NP_113659.3:p.Ser561=
NM_001382361.1:c.1683C>T	NP_001369290.1:p.Ser561=
NM_001382362.1:c.1695C>T	NP_001369291.1:p.Ser565=
NM_001382363.1:c.1143C>T	NP_001369292.1:p.Ser381=
NM_001382364.1:c.1155C>T	NP_001369293.1:p.Ser385=
NM_001382448.1:c.1683C>T	NP_001369377.1:p.Ser561=
NM_178443.3:c.1695C>T	NP_848537.1:p.Ser565=