Canonical Allele Identifier: CA381089395

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990520G>C (hg19) ; chr11:g.64223048G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223048G>C , CM000673.2:g.64223048G>C	GRCh38
NC_000011.9:g.63990520G>C , CM000673.1:g.63990520G>C	GRCh37
NC_000011.8:g.63747096G>C	NCBI36
NG_016360.1:g.21369G>C , LRG_180:g.21369G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1683G>C	ENSP00000279227.5:p.Arg561Ser
ENST00000540554.2:n.3195G>C
ENST00000541252.2:c.1131G>C	ENSP00000438885.2:p.Arg377Ser
ENST00000544997.6:c.1671G>C	ENSP00000445778.2:p.Arg557Ser
ENST00000545896.2:c.235G>C	ENSP00000440209.2:p.Val79Leu
ENST00000546255.2:n.1975G>C
ENST00000698845.1:c.*866G>C	ENSP00000513981.1:n.*866G>C
ENST00000698846.1:n.1917G>C
ENST00000698847.1:c.*1076G>C	ENSP00000513982.1:n.*1076G>C
ENST00000698850.1:n.3692G>C
ENST00000698852.1:c.1671G>C	ENSP00000513984.1:p.Arg557Ser
ENST00000698853.1:c.*900G>C	ENSP00000513985.1:n.*900G>C
ENST00000698854.1:c.*1001G>C	ENSP00000513986.1:n.*1001G>C
ENST00000698855.1:n.3323G>C
ENST00000698856.1:n.3017G>C
ENST00000698859.1:n.2181G>C
ENST00000698860.1:c.1683G>C	ENSP00000513988.1:p.Arg561Ser
ENST00000698861.1:c.1671G>C	ENSP00000513989.1:p.Arg557Ser
ENST00000698862.1:c.*967G>C	ENSP00000513990.1:n.*967G>C
ENST00000698863.1:c.1671G>C	ENSP00000513991.1:p.Arg557Ser
ENST00000698864.1:n.2232G>C
ENST00000698865.1:c.1692G>C	ENSP00000513992.1:p.Arg564Ser
ENST00000698866.1:c.*1459G>C	ENSP00000513993.1:n.*1459G>C
ENST00000698867.1:n.5646G>C
ENST00000698868.1:c.1536G>C	ENSP00000513994.1:p.Arg512Ser
ENST00000698869.1:c.1437G>C	ENSP00000513995.1:p.Arg479Ser
ENST00000698870.1:c.1671G>C	ENSP00000513996.1:p.Arg557Ser
ENST00000698871.1:n.2194G>C
ENST00000698872.1:c.*460G>C	ENSP00000513997.1:n.*460G>C
ENST00000698873.1:c.*866G>C	ENSP00000513998.1:n.*866G>C
ENST00000698874.1:c.1131G>C	ENSP00000513999.1:p.Arg377Ser
ENST00000698875.1:n.1531G>C
ENST00000698876.1:n.1719G>C
ENST00000698877.1:n.1239G>C
ENST00000698878.1:c.1665G>C	ENSP00000514000.1:p.Arg555Ser
ENST00000698880.1:c.1539G>C
ENST00000345728.10:c.1671G>C MANE Select	ENSP00000339950.5:p.Arg557Ser
ENST00000279227.9:c.1683G>C	ENSP00000279227.5:p.Arg561Ser
ENST00000345728.9:c.1671G>C	ENSP00000339950.5:p.Arg557Ser
ENST00000540554.1:n.307G>C
ENST00000545896.1:c.234G>C	ENSP00000440209.1:p.Arg78Ser
NM_031471.5:c.1671G>C	NP_113659.3:p.Arg557Ser
NM_178443.2:c.1683G>C , LRG_180t1:c.1683G>C	NP_848537.1:p.Arg561Ser
XM_011545294.1:c.1683G>C	XP_011543596.1:p.Arg561Ser
XM_011545295.1:c.1143G>C	XP_011543597.1:p.Arg381Ser
XM_011545296.1:c.1143G>C	XP_011543598.1:p.Arg381Ser
XM_011545294.3:c.1683G>C	XP_011543596.1:p.Arg561Ser
XM_011545295.2:c.1143G>C	XP_011543597.1:p.Arg381Ser
XM_017018398.2:c.1671G>C	XP_016873887.1:p.Arg557Ser
XM_017018399.1:c.1131G>C	XP_016873888.1:p.Arg377Ser
NM_031471.6:c.1671G>C MANE Select	NP_113659.3:p.Arg557Ser
NM_001382361.1:c.1671G>C	NP_001369290.1:p.Arg557Ser
NM_001382362.1:c.1683G>C	NP_001369291.1:p.Arg561Ser
NM_001382363.1:c.1131G>C	NP_001369292.1:p.Arg377Ser
NM_001382364.1:c.1143G>C	NP_001369293.1:p.Arg381Ser
NM_001382448.1:c.1671G>C	NP_001369377.1:p.Arg557Ser
NM_178443.3:c.1683G>C	NP_848537.1:p.Arg561Ser