Canonical Allele Identifier: CA381089882

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990611T>C (hg19) ; chr11:g.64223139T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223139T>C , CM000673.2:g.64223139T>C	GRCh38
NC_000011.9:g.63990611T>C , CM000673.1:g.63990611T>C	GRCh37
NC_000011.8:g.63747187T>C	NCBI36
NG_016360.1:g.21460T>C , LRG_180:g.21460T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1774T>C	ENSP00000279227.5:p.Trp592Arg
ENST00000540554.2:n.3286T>C
ENST00000541252.2:c.1222T>C	ENSP00000438885.2:p.Trp408Arg
ENST00000544997.6:c.1762T>C	ENSP00000445778.2:p.Trp588Arg
ENST00000545896.2:c.326T>C	ENSP00000440209.2:p.Leu109Pro
ENST00000546255.2:n.2066T>C
ENST00000698845.1:c.*957T>C	ENSP00000513981.1:n.*957T>C
ENST00000698846.1:n.2008T>C
ENST00000698847.1:c.*1167T>C	ENSP00000513982.1:n.*1167T>C
ENST00000698850.1:n.3783T>C
ENST00000698852.1:c.1762T>C	ENSP00000513984.1:p.Trp588Arg
ENST00000698853.1:c.*991T>C	ENSP00000513985.1:n.*991T>C
ENST00000698854.1:c.*1092T>C	ENSP00000513986.1:n.*1092T>C
ENST00000698855.1:n.3414T>C
ENST00000698856.1:n.3108T>C
ENST00000698859.1:n.2272T>C
ENST00000698860.1:c.1774T>C	ENSP00000513988.1:p.Trp592Arg
ENST00000698861.1:c.1762T>C	ENSP00000513989.1:p.Trp588Arg
ENST00000698862.1:c.*1058T>C	ENSP00000513990.1:n.*1058T>C
ENST00000698863.1:c.1762T>C	ENSP00000513991.1:p.Trp588Arg
ENST00000698864.1:n.2323T>C
ENST00000698865.1:c.1783T>C	ENSP00000513992.1:p.Trp595Arg
ENST00000698866.1:c.*1550T>C	ENSP00000513993.1:n.*1550T>C
ENST00000698867.1:n.5737T>C
ENST00000698868.1:c.1627T>C	ENSP00000513994.1:p.Trp543Arg
ENST00000698869.1:c.1528T>C	ENSP00000513995.1:p.Trp510Arg
ENST00000698870.1:c.1762T>C	ENSP00000513996.1:p.Trp588Arg
ENST00000698871.1:n.2285T>C
ENST00000698872.1:c.*551T>C	ENSP00000513997.1:n.*551T>C
ENST00000698873.1:c.*957T>C	ENSP00000513998.1:n.*957T>C
ENST00000698874.1:c.1222T>C	ENSP00000513999.1:p.Trp408Arg
ENST00000698875.1:n.1622T>C
ENST00000698876.1:n.1810T>C
ENST00000698877.1:n.1330T>C
ENST00000698878.1:c.1756T>C	ENSP00000514000.1:p.Trp586Arg
ENST00000698880.1:c.1630T>C
ENST00000345728.10:c.1762T>C MANE Select	ENSP00000339950.5:p.Trp588Arg
ENST00000279227.9:c.1774T>C	ENSP00000279227.5:p.Trp592Arg
ENST00000345728.9:c.1762T>C	ENSP00000339950.5:p.Trp588Arg
ENST00000545896.1:c.325T>C	ENSP00000440209.1:p.Trp109Arg
NM_031471.5:c.1762T>C	NP_113659.3:p.Trp588Arg
NM_178443.2:c.1774T>C , LRG_180t1:c.1774T>C	NP_848537.1:p.Trp592Arg
XM_011545294.1:c.1774T>C	XP_011543596.1:p.Trp592Arg
XM_011545295.1:c.1234T>C	XP_011543597.1:p.Trp412Arg
XM_011545296.1:c.1234T>C	XP_011543598.1:p.Trp412Arg
XM_011545294.3:c.1774T>C	XP_011543596.1:p.Trp592Arg
XM_011545295.2:c.1234T>C	XP_011543597.1:p.Trp412Arg
XM_017018398.2:c.1762T>C	XP_016873887.1:p.Trp588Arg
XM_017018399.1:c.1222T>C	XP_016873888.1:p.Trp408Arg
NM_031471.6:c.1762T>C MANE Select	NP_113659.3:p.Trp588Arg
NM_001382361.1:c.1762T>C	NP_001369290.1:p.Trp588Arg
NM_001382362.1:c.1774T>C	NP_001369291.1:p.Trp592Arg
NM_001382363.1:c.1222T>C	NP_001369292.1:p.Trp408Arg
NM_001382364.1:c.1234T>C	NP_001369293.1:p.Trp412Arg
NM_001382448.1:c.1762T>C	NP_001369377.1:p.Trp588Arg
NM_178443.3:c.1774T>C	NP_848537.1:p.Trp592Arg