Canonical Allele Identifier: CA2724430560

Gene: FERMT3

Linked Data

• dbSNP Id: rs2134885822

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220563_64220577del , CM000673.2:g.64220563_64220577del	GRCh38
NC_000011.9:g.63988035_63988049del , CM000673.1:g.63988035_63988049del	GRCh37
NC_000011.8:g.63744611_63744625del	NCBI36
NG_016360.1:g.18884_18898del , LRG_180:g.18884_18898del

Transcript Alleles

HGVS	Amino-acid change
ENST00000279227.10:c.1451_1465del	ENSP00000279227.5:p.Ser484_Gly488del
ENST00000540554.2:n.2617_2631del
ENST00000541252.2:c.899_913del	ENSP00000438885.2:p.Ser300_Gly304del
ENST00000541326.6:n.860_874del
ENST00000544997.6:c.1439_1453del	ENSP00000445778.2:p.Ser480_Gly484del
ENST00000545896.2:c.128_142del	ENSP00000440209.2:p.Ser43_Gly47del
ENST00000546255.2:n.1743_1757del
ENST00000698845.1:c.*634_*648del	ENSP00000513981.1:n.*634_*648del
ENST00000698846.1:n.1685_1699del
ENST00000698847.1:c.*844_*858del	ENSP00000513982.1:n.*844_*858del
ENST00000698849.1:n.559_573del
ENST00000698850.1:n.1207_1221del
ENST00000698852.1:c.1439_1453del	ENSP00000513984.1:p.Ser480_Gly484del
ENST00000698853.1:c.*668_*682del	ENSP00000513985.1:n.*668_*682del
ENST00000698854.1:c.*769_*783del	ENSP00000513986.1:n.*769_*783del
ENST00000698855.1:n.3091_3105del
ENST00000698856.1:n.2785_2799del
ENST00000698859.1:n.1603_1617del
ENST00000698860.1:c.1451_1465del	ENSP00000513988.1:p.Ser484_Gly488del
ENST00000698861.1:c.1439_1453del	ENSP00000513989.1:p.Ser480_Gly484del
ENST00000698862.1:c.*735_*749del	ENSP00000513990.1:n.*735_*749del
ENST00000698863.1:c.1439_1453del	ENSP00000513991.1:p.Ser480_Gly484del
ENST00000698864.1:n.1654_1668del
ENST00000698865.1:c.1460_1474del	ENSP00000513992.1:p.Ser487_Gly491del
ENST00000698866.1:c.*953_*967del	ENSP00000513993.1:n.*953_*967del
ENST00000698867.1:n.5414_5428del
ENST00000698868.1:c.1304_1318del	ENSP00000513994.1:p.Ser435_Gly439del
ENST00000698869.1:c.1311+237_1311+251del	ENSP00000513995.1:n.1311+237_1311+251del
ENST00000698870.1:c.1439_1453del	ENSP00000513996.1:p.Ser480_Gly484del
ENST00000698871.1:n.1962_1976del
ENST00000698872.1:c.*228_*242del	ENSP00000513997.1:n.*228_*242del
ENST00000698873.1:c.*634_*648del	ENSP00000513998.1:n.*634_*648del
ENST00000698874.1:c.899_913del	ENSP00000513999.1:p.Ser300_Gly304del
ENST00000698875.1:n.1299_1313del
ENST00000698876.1:n.1487_1501del
ENST00000698877.1:n.1007_1021del
ENST00000698878.1:c.1433_1447del	ENSP00000514000.1:p.Ser478_Gly482del
ENST00000698880.1:c.1307_1321del
ENST00000345728.10:c.1439_1453del MANE Select	ENSP00000339950.5:p.Ser480_Gly484del
ENST00000279227.9:c.1451_1465del	ENSP00000279227.5:p.Ser484_Gly488del
ENST00000345728.9:c.1439_1453del	ENSP00000339950.5:p.Ser480_Gly484del
ENST00000541326.5:n.855_869del
ENST00000545896.1:c.127_141del	ENSP00000440209.1:p.Val43_Ala47del
NM_031471.5:c.1439_1453del	NP_113659.3:p.Ser480_Gly484del
NM_178443.2:c.1451_1465del , LRG_180t1:c.1451_1465del	NP_848537.1:p.Ser484_Gly488del
XM_011545294.1:c.1451_1465del	XP_011543596.1:p.Ser484_Gly488del
XM_011545295.1:c.911_925del	XP_011543597.1:p.Ser304_Gly308del
XM_011545296.1:c.911_925del	XP_011543598.1:p.Ser304_Gly308del
XM_011545294.3:c.1451_1465del	XP_011543596.1:p.Ser484_Gly488del
XM_011545295.2:c.911_925del	XP_011543597.1:p.Ser304_Gly308del
XM_017018398.2:c.1439_1453del	XP_016873887.1:p.Ser480_Gly484del
XM_017018399.1:c.899_913del	XP_016873888.1:p.Ser300_Gly304del
NM_031471.6:c.1439_1453del MANE Select	NP_113659.3:p.Ser480_Gly484del
NM_001382361.1:c.1439_1453del	NP_001369290.1:p.Ser480_Gly484del
NM_001382362.1:c.1451_1465del	NP_001369291.1:p.Ser484_Gly488del
NM_001382363.1:c.899_913del	NP_001369292.1:p.Ser300_Gly304del
NM_001382364.1:c.911_925del	NP_001369293.1:p.Ser304_Gly308del
NM_001382448.1:c.1439_1453del	NP_001369377.1:p.Ser480_Gly484del
NM_178443.3:c.1451_1465del	NP_848537.1:p.Ser484_Gly488del