Canonical Allele Identifier: CA381087510

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987950T>G (hg19) ; chr11:g.64220478T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220478T>G , CM000673.2:g.64220478T>G	GRCh38
NC_000011.9:g.63987950T>G , CM000673.1:g.63987950T>G	GRCh37
NC_000011.8:g.63744526T>G	NCBI36
NG_016360.1:g.18799T>G , LRG_180:g.18799T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1366T>G	ENSP00000279227.5:p.Ser456Ala
ENST00000540554.2:n.2532T>G
ENST00000541252.2:c.814T>G	ENSP00000438885.2:p.Ser272Ala
ENST00000541326.6:n.775T>G
ENST00000544997.6:c.1354T>G	ENSP00000445778.2:p.Ser452Ala
ENST00000545896.2:c.43T>G	ENSP00000440209.2:p.Ser15Ala
ENST00000546255.2:n.1658T>G
ENST00000698845.1:c.*549T>G	ENSP00000513981.1:n.*549T>G
ENST00000698846.1:n.1600T>G
ENST00000698847.1:c.*759T>G	ENSP00000513982.1:n.*759T>G
ENST00000698848.1:n.652T>G
ENST00000698849.1:n.474T>G
ENST00000698850.1:n.1122T>G
ENST00000698852.1:c.1354T>G	ENSP00000513984.1:p.Ser452Ala
ENST00000698853.1:c.*583T>G	ENSP00000513985.1:n.*583T>G
ENST00000698854.1:c.*684T>G	ENSP00000513986.1:n.*684T>G
ENST00000698855.1:n.3006T>G
ENST00000698856.1:n.2700T>G
ENST00000698859.1:n.1518T>G
ENST00000698860.1:c.1366T>G	ENSP00000513988.1:p.Ser456Ala
ENST00000698861.1:c.1354T>G	ENSP00000513989.1:p.Ser452Ala
ENST00000698862.1:c.*650T>G	ENSP00000513990.1:n.*650T>G
ENST00000698863.1:c.1354T>G	ENSP00000513991.1:p.Ser452Ala
ENST00000698864.1:n.1569T>G
ENST00000698865.1:c.1375T>G	ENSP00000513992.1:p.Ser459Ala
ENST00000698866.1:c.*868T>G	ENSP00000513993.1:n.*868T>G
ENST00000698867.1:n.5329T>G
ENST00000698868.1:c.1219T>G	ENSP00000513994.1:p.Ser407Ala
ENST00000698869.1:c.1311+152T>G	ENSP00000513995.1:n.1311+152T>G
ENST00000698870.1:c.1354T>G	ENSP00000513996.1:p.Ser452Ala
ENST00000698871.1:n.1877T>G
ENST00000698872.1:c.*143T>G	ENSP00000513997.1:n.*143T>G
ENST00000698873.1:c.*549T>G	ENSP00000513998.1:n.*549T>G
ENST00000698874.1:c.814T>G	ENSP00000513999.1:p.Ser272Ala
ENST00000698875.1:n.1214T>G
ENST00000698876.1:n.1402T>G
ENST00000698877.1:n.922T>G
ENST00000698878.1:c.1348T>G	ENSP00000514000.1:p.Ser450Ala
ENST00000698880.1:c.1222T>G
ENST00000345728.10:c.1354T>G MANE Select	ENSP00000339950.5:p.Ser452Ala
ENST00000279227.9:c.1366T>G	ENSP00000279227.5:p.Ser456Ala
ENST00000345728.9:c.1354T>G	ENSP00000339950.5:p.Ser452Ala
ENST00000541326.5:n.770T>G
ENST00000545896.1:c.42T>G	ENSP00000440209.1:p.Pro14=
NM_031471.5:c.1354T>G	NP_113659.3:p.Ser452Ala
NM_178443.2:c.1366T>G , LRG_180t1:c.1366T>G	NP_848537.1:p.Ser456Ala
XM_011545294.1:c.1366T>G	XP_011543596.1:p.Ser456Ala
XM_011545295.1:c.826T>G	XP_011543597.1:p.Ser276Ala
XM_011545296.1:c.826T>G	XP_011543598.1:p.Ser276Ala
XM_011545294.3:c.1366T>G	XP_011543596.1:p.Ser456Ala
XM_011545295.2:c.826T>G	XP_011543597.1:p.Ser276Ala
XM_017018398.2:c.1354T>G	XP_016873887.1:p.Ser452Ala
XM_017018399.1:c.814T>G	XP_016873888.1:p.Ser272Ala
NM_031471.6:c.1354T>G MANE Select	NP_113659.3:p.Ser452Ala
NM_001382361.1:c.1354T>G	NP_001369290.1:p.Ser452Ala
NM_001382362.1:c.1366T>G	NP_001369291.1:p.Ser456Ala
NM_001382363.1:c.814T>G	NP_001369292.1:p.Ser272Ala
NM_001382364.1:c.826T>G	NP_001369293.1:p.Ser276Ala
NM_001382448.1:c.1354T>G	NP_001369377.1:p.Ser452Ala
NM_178443.3:c.1366T>G	NP_848537.1:p.Ser456Ala