Canonical Allele Identifier: CA381087521

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987953A>T (hg19) ; chr11:g.64220481A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220481A>T , CM000673.2:g.64220481A>T	GRCh38
NC_000011.9:g.63987953A>T , CM000673.1:g.63987953A>T	GRCh37
NC_000011.8:g.63744529A>T	NCBI36
NG_016360.1:g.18802A>T , LRG_180:g.18802A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1369A>T	ENSP00000279227.5:p.Lys457Ter
ENST00000540554.2:n.2535A>T
ENST00000541252.2:c.817A>T	ENSP00000438885.2:p.Lys273Ter
ENST00000541326.6:n.778A>T
ENST00000544997.6:c.1357A>T	ENSP00000445778.2:p.Lys453Ter
ENST00000545896.2:c.46A>T	ENSP00000440209.2:p.Lys16Ter
ENST00000546255.2:n.1661A>T
ENST00000698845.1:c.*552A>T	ENSP00000513981.1:n.*552A>T
ENST00000698846.1:n.1603A>T
ENST00000698847.1:c.*762A>T	ENSP00000513982.1:n.*762A>T
ENST00000698848.1:n.655A>T
ENST00000698849.1:n.477A>T
ENST00000698850.1:n.1125A>T
ENST00000698852.1:c.1357A>T	ENSP00000513984.1:p.Lys453Ter
ENST00000698853.1:c.*586A>T	ENSP00000513985.1:n.*586A>T
ENST00000698854.1:c.*687A>T	ENSP00000513986.1:n.*687A>T
ENST00000698855.1:n.3009A>T
ENST00000698856.1:n.2703A>T
ENST00000698859.1:n.1521A>T
ENST00000698860.1:c.1369A>T	ENSP00000513988.1:p.Lys457Ter
ENST00000698861.1:c.1357A>T	ENSP00000513989.1:p.Lys453Ter
ENST00000698862.1:c.*653A>T	ENSP00000513990.1:n.*653A>T
ENST00000698863.1:c.1357A>T	ENSP00000513991.1:p.Lys453Ter
ENST00000698864.1:n.1572A>T
ENST00000698865.1:c.1378A>T	ENSP00000513992.1:p.Lys460Ter
ENST00000698866.1:c.*871A>T	ENSP00000513993.1:n.*871A>T
ENST00000698867.1:n.5332A>T
ENST00000698868.1:c.1222A>T	ENSP00000513994.1:p.Lys408Ter
ENST00000698869.1:c.1311+155A>T	ENSP00000513995.1:n.1311+155A>T
ENST00000698870.1:c.1357A>T	ENSP00000513996.1:p.Lys453Ter
ENST00000698871.1:n.1880A>T
ENST00000698872.1:c.*146A>T	ENSP00000513997.1:n.*146A>T
ENST00000698873.1:c.*552A>T	ENSP00000513998.1:n.*552A>T
ENST00000698874.1:c.817A>T	ENSP00000513999.1:p.Lys273Ter
ENST00000698875.1:n.1217A>T
ENST00000698876.1:n.1405A>T
ENST00000698877.1:n.925A>T
ENST00000698878.1:c.1351A>T	ENSP00000514000.1:p.Lys451Ter
ENST00000698880.1:c.1225A>T
ENST00000345728.10:c.1357A>T MANE Select	ENSP00000339950.5:p.Lys453Ter
ENST00000279227.9:c.1369A>T	ENSP00000279227.5:p.Lys457Ter
ENST00000345728.9:c.1357A>T	ENSP00000339950.5:p.Lys453Ter
ENST00000541326.5:n.773A>T
ENST00000545896.1:c.45A>T	ENSP00000440209.1:p.Pro15=
NM_031471.5:c.1357A>T	NP_113659.3:p.Lys453Ter
NM_178443.2:c.1369A>T , LRG_180t1:c.1369A>T	NP_848537.1:p.Lys457Ter
XM_011545294.1:c.1369A>T	XP_011543596.1:p.Lys457Ter
XM_011545295.1:c.829A>T	XP_011543597.1:p.Lys277Ter
XM_011545296.1:c.829A>T	XP_011543598.1:p.Lys277Ter
XM_011545294.3:c.1369A>T	XP_011543596.1:p.Lys457Ter
XM_011545295.2:c.829A>T	XP_011543597.1:p.Lys277Ter
XM_017018398.2:c.1357A>T	XP_016873887.1:p.Lys453Ter
XM_017018399.1:c.817A>T	XP_016873888.1:p.Lys273Ter
NM_031471.6:c.1357A>T MANE Select	NP_113659.3:p.Lys453Ter
NM_001382361.1:c.1357A>T	NP_001369290.1:p.Lys453Ter
NM_001382362.1:c.1369A>T	NP_001369291.1:p.Lys457Ter
NM_001382363.1:c.817A>T	NP_001369292.1:p.Lys273Ter
NM_001382364.1:c.829A>T	NP_001369293.1:p.Lys277Ter
NM_001382448.1:c.1357A>T	NP_001369377.1:p.Lys453Ter
NM_178443.3:c.1369A>T	NP_848537.1:p.Lys457Ter