Canonical Allele Identifier: CA381088381

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988105T>C (hg19) ; chr11:g.64220633T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220633T>C , CM000673.2:g.64220633T>C	GRCh38
NC_000011.9:g.63988105T>C , CM000673.1:g.63988105T>C	GRCh37
NC_000011.8:g.63744681T>C	NCBI36
NG_016360.1:g.18954T>C , LRG_180:g.18954T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1521T>C	ENSP00000279227.5:p.Val507=
ENST00000540554.2:n.2687T>C
ENST00000541252.2:c.969T>C	ENSP00000438885.2:p.Val323=
ENST00000541326.6:n.930T>C
ENST00000544997.6:c.1509T>C	ENSP00000445778.2:p.Val503=
ENST00000545896.2:c.198T>C	ENSP00000440209.2:p.Val66=
ENST00000546255.2:n.1813T>C
ENST00000698845.1:c.*704T>C	ENSP00000513981.1:n.*704T>C
ENST00000698846.1:n.1755T>C
ENST00000698847.1:c.*914T>C	ENSP00000513982.1:n.*914T>C
ENST00000698849.1:n.629T>C
ENST00000698850.1:n.1277T>C
ENST00000698852.1:c.1509T>C	ENSP00000513984.1:p.Val503=
ENST00000698853.1:c.*738T>C	ENSP00000513985.1:n.*738T>C
ENST00000698854.1:c.*839T>C	ENSP00000513986.1:n.*839T>C
ENST00000698855.1:n.3161T>C
ENST00000698856.1:n.2855T>C
ENST00000698859.1:n.1673T>C
ENST00000698860.1:c.1521T>C	ENSP00000513988.1:p.Val507=
ENST00000698861.1:c.1509T>C	ENSP00000513989.1:p.Val503=
ENST00000698862.1:c.*805T>C	ENSP00000513990.1:n.*805T>C
ENST00000698863.1:c.1509T>C	ENSP00000513991.1:p.Val503=
ENST00000698864.1:n.1724T>C
ENST00000698865.1:c.1530T>C	ENSP00000513992.1:p.Val510=
ENST00000698866.1:c.*1023T>C	ENSP00000513993.1:n.*1023T>C
ENST00000698867.1:n.5484T>C
ENST00000698868.1:c.1374T>C	ENSP00000513994.1:p.Val458=
ENST00000698869.1:c.1311+307T>C	ENSP00000513995.1:n.1311+307T>C
ENST00000698870.1:c.1509T>C	ENSP00000513996.1:p.Val503=
ENST00000698871.1:n.2032T>C
ENST00000698872.1:c.*298T>C	ENSP00000513997.1:n.*298T>C
ENST00000698873.1:c.*704T>C	ENSP00000513998.1:n.*704T>C
ENST00000698874.1:c.969T>C	ENSP00000513999.1:p.Val323=
ENST00000698875.1:n.1369T>C
ENST00000698876.1:n.1557T>C
ENST00000698877.1:n.1077T>C
ENST00000698878.1:c.1503T>C	ENSP00000514000.1:p.Val501=
ENST00000698880.1:c.1377T>C
ENST00000345728.10:c.1509T>C MANE Select	ENSP00000339950.5:p.Val503=
ENST00000279227.9:c.1521T>C	ENSP00000279227.5:p.Val507=
ENST00000345728.9:c.1509T>C	ENSP00000339950.5:p.Val503=
ENST00000545896.1:c.197T>C	ENSP00000440209.1:p.Leu66Ser
NM_031471.5:c.1509T>C	NP_113659.3:p.Val503=
NM_178443.2:c.1521T>C , LRG_180t1:c.1521T>C	NP_848537.1:p.Val507=
XM_011545294.1:c.1521T>C	XP_011543596.1:p.Val507=
XM_011545295.1:c.981T>C	XP_011543597.1:p.Val327=
XM_011545296.1:c.981T>C	XP_011543598.1:p.Val327=
XM_011545294.3:c.1521T>C	XP_011543596.1:p.Val507=
XM_011545295.2:c.981T>C	XP_011543597.1:p.Val327=
XM_017018398.2:c.1509T>C	XP_016873887.1:p.Val503=
XM_017018399.1:c.969T>C	XP_016873888.1:p.Val323=
NM_031471.6:c.1509T>C MANE Select	NP_113659.3:p.Val503=
NM_001382361.1:c.1509T>C	NP_001369290.1:p.Val503=
NM_001382362.1:c.1521T>C	NP_001369291.1:p.Val507=
NM_001382363.1:c.969T>C	NP_001369292.1:p.Val323=
NM_001382364.1:c.981T>C	NP_001369293.1:p.Val327=
NM_001382448.1:c.1509T>C	NP_001369377.1:p.Val503=
NM_178443.3:c.1521T>C	NP_848537.1:p.Val507=