Canonical Allele Identifier: CA381088117

Gene: FERMT3

Linked Data

• dbSNP Id: rs1459394997
• gnomAD v2: 11-63988076-G-A
• MyVariant Identifiers: chr11:g.63988076G>A (hg19) ; chr11:g.64220604G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220604G>A , CM000673.2:g.64220604G>A	GRCh38
NC_000011.9:g.63988076G>A , CM000673.1:g.63988076G>A	GRCh37
NC_000011.8:g.63744652G>A	NCBI36
NG_016360.1:g.18925G>A , LRG_180:g.18925G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1492G>A	ENSP00000279227.5:p.Ala498Thr
ENST00000540554.2:n.2658G>A
ENST00000541252.2:c.940G>A	ENSP00000438885.2:p.Ala314Thr
ENST00000541326.6:n.901G>A
ENST00000544997.6:c.1480G>A	ENSP00000445778.2:p.Ala494Thr
ENST00000545896.2:c.169G>A	ENSP00000440209.2:p.Ala57Thr
ENST00000546255.2:n.1784G>A
ENST00000698845.1:c.*675G>A	ENSP00000513981.1:n.*675G>A
ENST00000698846.1:n.1726G>A
ENST00000698847.1:c.*885G>A	ENSP00000513982.1:n.*885G>A
ENST00000698849.1:n.600G>A
ENST00000698850.1:n.1248G>A
ENST00000698852.1:c.1480G>A	ENSP00000513984.1:p.Ala494Thr
ENST00000698853.1:c.*709G>A	ENSP00000513985.1:n.*709G>A
ENST00000698854.1:c.*810G>A	ENSP00000513986.1:n.*810G>A
ENST00000698855.1:n.3132G>A
ENST00000698856.1:n.2826G>A
ENST00000698859.1:n.1644G>A
ENST00000698860.1:c.1492G>A	ENSP00000513988.1:p.Ala498Thr
ENST00000698861.1:c.1480G>A	ENSP00000513989.1:p.Ala494Thr
ENST00000698862.1:c.*776G>A	ENSP00000513990.1:n.*776G>A
ENST00000698863.1:c.1480G>A	ENSP00000513991.1:p.Ala494Thr
ENST00000698864.1:n.1695G>A
ENST00000698865.1:c.1501G>A	ENSP00000513992.1:p.Ala501Thr
ENST00000698866.1:c.*994G>A	ENSP00000513993.1:n.*994G>A
ENST00000698867.1:n.5455G>A
ENST00000698868.1:c.1345G>A	ENSP00000513994.1:p.Ala449Thr
ENST00000698869.1:c.1311+278G>A	ENSP00000513995.1:n.1311+278G>A
ENST00000698870.1:c.1480G>A	ENSP00000513996.1:p.Ala494Thr
ENST00000698871.1:n.2003G>A
ENST00000698872.1:c.*269G>A	ENSP00000513997.1:n.*269G>A
ENST00000698873.1:c.*675G>A	ENSP00000513998.1:n.*675G>A
ENST00000698874.1:c.940G>A	ENSP00000513999.1:p.Ala314Thr
ENST00000698875.1:n.1340G>A
ENST00000698876.1:n.1528G>A
ENST00000698877.1:n.1048G>A
ENST00000698878.1:c.1474G>A	ENSP00000514000.1:p.Ala492Thr
ENST00000698880.1:c.1348G>A
ENST00000345728.10:c.1480G>A MANE Select	ENSP00000339950.5:p.Ala494Thr
ENST00000279227.9:c.1492G>A	ENSP00000279227.5:p.Ala498Thr
ENST00000345728.9:c.1480G>A	ENSP00000339950.5:p.Ala494Thr
ENST00000545896.1:c.168G>A	ENSP00000440209.1:p.Leu56=
NM_031471.5:c.1480G>A	NP_113659.3:p.Ala494Thr
NM_178443.2:c.1492G>A , LRG_180t1:c.1492G>A	NP_848537.1:p.Ala498Thr
XM_011545294.1:c.1492G>A	XP_011543596.1:p.Ala498Thr
XM_011545295.1:c.952G>A	XP_011543597.1:p.Ala318Thr
XM_011545296.1:c.952G>A	XP_011543598.1:p.Ala318Thr
XM_011545294.3:c.1492G>A	XP_011543596.1:p.Ala498Thr
XM_011545295.2:c.952G>A	XP_011543597.1:p.Ala318Thr
XM_017018398.2:c.1480G>A	XP_016873887.1:p.Ala494Thr
XM_017018399.1:c.940G>A	XP_016873888.1:p.Ala314Thr
NM_031471.6:c.1480G>A MANE Select	NP_113659.3:p.Ala494Thr
NM_001382361.1:c.1480G>A	NP_001369290.1:p.Ala494Thr
NM_001382362.1:c.1492G>A	NP_001369291.1:p.Ala498Thr
NM_001382363.1:c.940G>A	NP_001369292.1:p.Ala314Thr
NM_001382364.1:c.952G>A	NP_001369293.1:p.Ala318Thr
NM_001382448.1:c.1480G>A	NP_001369377.1:p.Ala494Thr
NM_178443.3:c.1492G>A	NP_848537.1:p.Ala498Thr