Canonical Allele Identifier: CA381087595

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987978G>C (hg19) ; chr11:g.64220506G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220506G>C , CM000673.2:g.64220506G>C	GRCh38
NC_000011.9:g.63987978G>C , CM000673.1:g.63987978G>C	GRCh37
NC_000011.8:g.63744554G>C	NCBI36
NG_016360.1:g.18827G>C , LRG_180:g.18827G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1394G>C	ENSP00000279227.5:p.Ser465Thr
ENST00000540554.2:n.2560G>C
ENST00000541252.2:c.842G>C	ENSP00000438885.2:p.Ser281Thr
ENST00000541326.6:n.803G>C
ENST00000544997.6:c.1382G>C	ENSP00000445778.2:p.Ser461Thr
ENST00000545896.2:c.71G>C	ENSP00000440209.2:p.Ser24Thr
ENST00000546255.2:n.1686G>C
ENST00000698845.1:c.*577G>C	ENSP00000513981.1:n.*577G>C
ENST00000698846.1:n.1628G>C
ENST00000698847.1:c.*787G>C	ENSP00000513982.1:n.*787G>C
ENST00000698849.1:n.502G>C
ENST00000698850.1:n.1150G>C
ENST00000698852.1:c.1382G>C	ENSP00000513984.1:p.Ser461Thr
ENST00000698853.1:c.*611G>C	ENSP00000513985.1:n.*611G>C
ENST00000698854.1:c.*712G>C	ENSP00000513986.1:n.*712G>C
ENST00000698855.1:n.3034G>C
ENST00000698856.1:n.2728G>C
ENST00000698859.1:n.1546G>C
ENST00000698860.1:c.1394G>C	ENSP00000513988.1:p.Ser465Thr
ENST00000698861.1:c.1382G>C	ENSP00000513989.1:p.Ser461Thr
ENST00000698862.1:c.*678G>C	ENSP00000513990.1:n.*678G>C
ENST00000698863.1:c.1382G>C	ENSP00000513991.1:p.Ser461Thr
ENST00000698864.1:n.1597G>C
ENST00000698865.1:c.1403G>C	ENSP00000513992.1:p.Ser468Thr
ENST00000698866.1:c.*896G>C	ENSP00000513993.1:n.*896G>C
ENST00000698867.1:n.5357G>C
ENST00000698868.1:c.1247G>C	ENSP00000513994.1:p.Ser416Thr
ENST00000698869.1:c.1311+180G>C	ENSP00000513995.1:n.1311+180G>C
ENST00000698870.1:c.1382G>C	ENSP00000513996.1:p.Ser461Thr
ENST00000698871.1:n.1905G>C
ENST00000698872.1:c.*171G>C	ENSP00000513997.1:n.*171G>C
ENST00000698873.1:c.*577G>C	ENSP00000513998.1:n.*577G>C
ENST00000698874.1:c.842G>C	ENSP00000513999.1:p.Ser281Thr
ENST00000698875.1:n.1242G>C
ENST00000698876.1:n.1430G>C
ENST00000698877.1:n.950G>C
ENST00000698878.1:c.1376G>C	ENSP00000514000.1:p.Ser459Thr
ENST00000698880.1:c.1250G>C
ENST00000345728.10:c.1382G>C MANE Select	ENSP00000339950.5:p.Ser461Thr
ENST00000279227.9:c.1394G>C	ENSP00000279227.5:p.Ser465Thr
ENST00000345728.9:c.1382G>C	ENSP00000339950.5:p.Ser461Thr
ENST00000541326.5:n.798G>C
ENST00000545896.1:c.70G>C	ENSP00000440209.1:p.Ala24Pro
NM_031471.5:c.1382G>C	NP_113659.3:p.Ser461Thr
NM_178443.2:c.1394G>C , LRG_180t1:c.1394G>C	NP_848537.1:p.Ser465Thr
XM_011545294.1:c.1394G>C	XP_011543596.1:p.Ser465Thr
XM_011545295.1:c.854G>C	XP_011543597.1:p.Ser285Thr
XM_011545296.1:c.854G>C	XP_011543598.1:p.Ser285Thr
XM_011545294.3:c.1394G>C	XP_011543596.1:p.Ser465Thr
XM_011545295.2:c.854G>C	XP_011543597.1:p.Ser285Thr
XM_017018398.2:c.1382G>C	XP_016873887.1:p.Ser461Thr
XM_017018399.1:c.842G>C	XP_016873888.1:p.Ser281Thr
NM_031471.6:c.1382G>C MANE Select	NP_113659.3:p.Ser461Thr
NM_001382361.1:c.1382G>C	NP_001369290.1:p.Ser461Thr
NM_001382362.1:c.1394G>C	NP_001369291.1:p.Ser465Thr
NM_001382363.1:c.842G>C	NP_001369292.1:p.Ser281Thr
NM_001382364.1:c.854G>C	NP_001369293.1:p.Ser285Thr
NM_001382448.1:c.1382G>C	NP_001369377.1:p.Ser461Thr
NM_178443.3:c.1394G>C	NP_848537.1:p.Ser465Thr