Canonical Allele Identifier: CA381089467

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990534G>C (hg19) ; chr11:g.64223062G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223062G>C , CM000673.2:g.64223062G>C	GRCh38
NC_000011.9:g.63990534G>C , CM000673.1:g.63990534G>C	GRCh37
NC_000011.8:g.63747110G>C	NCBI36
NG_016360.1:g.21383G>C , LRG_180:g.21383G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1697G>C	ENSP00000279227.5:p.Arg566Thr
ENST00000540554.2:n.3209G>C
ENST00000541252.2:c.1145G>C	ENSP00000438885.2:p.Arg382Thr
ENST00000544997.6:c.1685G>C	ENSP00000445778.2:p.Arg562Thr
ENST00000545896.2:c.249G>C	ENSP00000440209.2:p.Gln83His
ENST00000546255.2:n.1989G>C
ENST00000698845.1:c.*880G>C	ENSP00000513981.1:n.*880G>C
ENST00000698846.1:n.1931G>C
ENST00000698847.1:c.*1090G>C	ENSP00000513982.1:n.*1090G>C
ENST00000698850.1:n.3706G>C
ENST00000698852.1:c.1685G>C	ENSP00000513984.1:p.Arg562Thr
ENST00000698853.1:c.*914G>C	ENSP00000513985.1:n.*914G>C
ENST00000698854.1:c.*1015G>C	ENSP00000513986.1:n.*1015G>C
ENST00000698855.1:n.3337G>C
ENST00000698856.1:n.3031G>C
ENST00000698859.1:n.2195G>C
ENST00000698860.1:c.1697G>C	ENSP00000513988.1:p.Arg566Thr
ENST00000698861.1:c.1685G>C	ENSP00000513989.1:p.Arg562Thr
ENST00000698862.1:c.*981G>C	ENSP00000513990.1:n.*981G>C
ENST00000698863.1:c.1685G>C	ENSP00000513991.1:p.Arg562Thr
ENST00000698864.1:n.2246G>C
ENST00000698865.1:c.1706G>C	ENSP00000513992.1:p.Arg569Thr
ENST00000698866.1:c.*1473G>C	ENSP00000513993.1:n.*1473G>C
ENST00000698867.1:n.5660G>C
ENST00000698868.1:c.1550G>C	ENSP00000513994.1:p.Arg517Thr
ENST00000698869.1:c.1451G>C	ENSP00000513995.1:p.Arg484Thr
ENST00000698870.1:c.1685G>C	ENSP00000513996.1:p.Arg562Thr
ENST00000698871.1:n.2208G>C
ENST00000698872.1:c.*474G>C	ENSP00000513997.1:n.*474G>C
ENST00000698873.1:c.*880G>C	ENSP00000513998.1:n.*880G>C
ENST00000698874.1:c.1145G>C	ENSP00000513999.1:p.Arg382Thr
ENST00000698875.1:n.1545G>C
ENST00000698876.1:n.1733G>C
ENST00000698877.1:n.1253G>C
ENST00000698878.1:c.1679G>C	ENSP00000514000.1:p.Arg560Thr
ENST00000698880.1:c.1553G>C
ENST00000345728.10:c.1685G>C MANE Select	ENSP00000339950.5:p.Arg562Thr
ENST00000279227.9:c.1697G>C	ENSP00000279227.5:p.Arg566Thr
ENST00000345728.9:c.1685G>C	ENSP00000339950.5:p.Arg562Thr
ENST00000540554.1:n.321G>C
ENST00000545896.1:c.248G>C	ENSP00000440209.1:p.Arg83Thr
NM_031471.5:c.1685G>C	NP_113659.3:p.Arg562Thr
NM_178443.2:c.1697G>C , LRG_180t1:c.1697G>C	NP_848537.1:p.Arg566Thr
XM_011545294.1:c.1697G>C	XP_011543596.1:p.Arg566Thr
XM_011545295.1:c.1157G>C	XP_011543597.1:p.Arg386Thr
XM_011545296.1:c.1157G>C	XP_011543598.1:p.Arg386Thr
XM_011545294.3:c.1697G>C	XP_011543596.1:p.Arg566Thr
XM_011545295.2:c.1157G>C	XP_011543597.1:p.Arg386Thr
XM_017018398.2:c.1685G>C	XP_016873887.1:p.Arg562Thr
XM_017018399.1:c.1145G>C	XP_016873888.1:p.Arg382Thr
NM_031471.6:c.1685G>C MANE Select	NP_113659.3:p.Arg562Thr
NM_001382361.1:c.1685G>C	NP_001369290.1:p.Arg562Thr
NM_001382362.1:c.1697G>C	NP_001369291.1:p.Arg566Thr
NM_001382363.1:c.1145G>C	NP_001369292.1:p.Arg382Thr
NM_001382364.1:c.1157G>C	NP_001369293.1:p.Arg386Thr
NM_001382448.1:c.1685G>C	NP_001369377.1:p.Arg562Thr
NM_178443.3:c.1697G>C	NP_848537.1:p.Arg566Thr