Canonical Allele Identifier: CA381087440

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64220462-T-C
• MyVariant Identifiers: chr11:g.63987934T>C (hg19) ; chr11:g.64220462T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220462T>C , CM000673.2:g.64220462T>C	GRCh38
NC_000011.9:g.63987934T>C , CM000673.1:g.63987934T>C	GRCh37
NC_000011.8:g.63744510T>C	NCBI36
NG_016360.1:g.18783T>C , LRG_180:g.18783T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1350T>C	ENSP00000279227.5:p.Ala450=
ENST00000540554.2:n.2516T>C
ENST00000541252.2:c.798T>C	ENSP00000438885.2:p.Ala266=
ENST00000541326.6:n.759T>C
ENST00000544997.6:c.1338T>C	ENSP00000445778.2:p.Ala446=
ENST00000545896.2:c.27T>C	ENSP00000440209.2:p.Ala9=
ENST00000546255.2:n.1642T>C
ENST00000698845.1:c.*533T>C	ENSP00000513981.1:n.*533T>C
ENST00000698846.1:n.1584T>C
ENST00000698847.1:c.*743T>C	ENSP00000513982.1:n.*743T>C
ENST00000698848.1:n.636T>C
ENST00000698849.1:n.458T>C
ENST00000698850.1:n.1106T>C
ENST00000698852.1:c.1338T>C	ENSP00000513984.1:p.Ala446=
ENST00000698853.1:c.*567T>C	ENSP00000513985.1:n.*567T>C
ENST00000698854.1:c.*668T>C	ENSP00000513986.1:n.*668T>C
ENST00000698855.1:n.2990T>C
ENST00000698856.1:n.2684T>C
ENST00000698859.1:n.1502T>C
ENST00000698860.1:c.1350T>C	ENSP00000513988.1:p.Ala450=
ENST00000698861.1:c.1338T>C	ENSP00000513989.1:p.Ala446=
ENST00000698862.1:c.*634T>C	ENSP00000513990.1:n.*634T>C
ENST00000698863.1:c.1338T>C	ENSP00000513991.1:p.Ala446=
ENST00000698864.1:n.1553T>C
ENST00000698865.1:c.1359T>C	ENSP00000513992.1:p.Ala453=
ENST00000698866.1:c.*852T>C	ENSP00000513993.1:n.*852T>C
ENST00000698867.1:n.5313T>C
ENST00000698868.1:c.1203T>C	ENSP00000513994.1:p.Ala401=
ENST00000698869.1:c.1311+136T>C	ENSP00000513995.1:n.1311+136T>C
ENST00000698870.1:c.1338T>C	ENSP00000513996.1:p.Ala446=
ENST00000698871.1:n.1861T>C
ENST00000698872.1:c.*127T>C	ENSP00000513997.1:n.*127T>C
ENST00000698873.1:c.*533T>C	ENSP00000513998.1:n.*533T>C
ENST00000698874.1:c.798T>C	ENSP00000513999.1:p.Ala266=
ENST00000698875.1:n.1198T>C
ENST00000698876.1:n.1386T>C
ENST00000698877.1:n.906T>C
ENST00000698878.1:c.1332T>C	ENSP00000514000.1:p.Ala444=
ENST00000698880.1:c.1206T>C
ENST00000345728.10:c.1338T>C MANE Select	ENSP00000339950.5:p.Ala446=
ENST00000279227.9:c.1350T>C	ENSP00000279227.5:p.Ala450=
ENST00000345728.9:c.1338T>C	ENSP00000339950.5:p.Ala446=
ENST00000541326.5:n.754T>C
ENST00000545896.1:c.26T>C	ENSP00000440209.1:p.Leu9Pro
NM_031471.5:c.1338T>C	NP_113659.3:p.Ala446=
NM_178443.2:c.1350T>C , LRG_180t1:c.1350T>C	NP_848537.1:p.Ala450=
XM_011545294.1:c.1350T>C	XP_011543596.1:p.Ala450=
XM_011545295.1:c.810T>C	XP_011543597.1:p.Ala270=
XM_011545296.1:c.810T>C	XP_011543598.1:p.Ala270=
XM_011545294.3:c.1350T>C	XP_011543596.1:p.Ala450=
XM_011545295.2:c.810T>C	XP_011543597.1:p.Ala270=
XM_017018398.2:c.1338T>C	XP_016873887.1:p.Ala446=
XM_017018399.1:c.798T>C	XP_016873888.1:p.Ala266=
NM_031471.6:c.1338T>C MANE Select	NP_113659.3:p.Ala446=
NM_001382361.1:c.1338T>C	NP_001369290.1:p.Ala446=
NM_001382362.1:c.1350T>C	NP_001369291.1:p.Ala450=
NM_001382363.1:c.798T>C	NP_001369292.1:p.Ala266=
NM_001382364.1:c.810T>C	NP_001369293.1:p.Ala270=
NM_001382448.1:c.1338T>C	NP_001369377.1:p.Ala446=
NM_178443.3:c.1350T>C	NP_848537.1:p.Ala450=