Canonical Allele Identifier: CA381087001

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987717C>G (hg19) ; chr11:g.64220245C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220245C>G , CM000673.2:g.64220245C>G	GRCh38
NC_000011.9:g.63987717C>G , CM000673.1:g.63987717C>G	GRCh37
NC_000011.8:g.63744293C>G	NCBI36
NG_016360.1:g.18566C>G , LRG_180:g.18566C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1242C>G	ENSP00000279227.5:p.Asn414Lys
ENST00000540554.2:n.2299C>G
ENST00000541252.2:c.690C>G	ENSP00000438885.2:p.Asn230Lys
ENST00000541326.6:n.542C>G
ENST00000544997.6:c.1230C>G	ENSP00000445778.2:p.Asn410Lys
ENST00000546255.2:n.1425C>G
ENST00000698845.1:c.*425C>G	ENSP00000513981.1:n.*425C>G
ENST00000698846.1:n.1367C>G
ENST00000698847.1:c.*635C>G	ENSP00000513982.1:n.*635C>G
ENST00000698848.1:n.419C>G
ENST00000698849.1:n.350C>G
ENST00000698850.1:n.889C>G
ENST00000698852.1:c.1230C>G	ENSP00000513984.1:p.Asn410Lys
ENST00000698853.1:c.*459C>G	ENSP00000513985.1:n.*459C>G
ENST00000698854.1:c.*560C>G	ENSP00000513986.1:n.*560C>G
ENST00000698855.1:n.2882C>G
ENST00000698856.1:n.2467C>G
ENST00000698859.1:n.1394C>G
ENST00000698860.1:c.1242C>G	ENSP00000513988.1:p.Asn414Lys
ENST00000698861.1:c.1230C>G	ENSP00000513989.1:p.Asn410Lys
ENST00000698862.1:c.*526C>G	ENSP00000513990.1:n.*526C>G
ENST00000698863.1:c.1230C>G	ENSP00000513991.1:p.Asn410Lys
ENST00000698864.1:n.1336C>G
ENST00000698865.1:c.1251C>G	ENSP00000513992.1:p.Asn417Lys
ENST00000698866.1:c.*635C>G	ENSP00000513993.1:n.*635C>G
ENST00000698867.1:n.5205C>G
ENST00000698868.1:c.1095C>G	ENSP00000513994.1:p.Asn365Lys
ENST00000698869.1:c.1230C>G	ENSP00000513995.1:p.Asn410Lys
ENST00000698870.1:c.1230C>G	ENSP00000513996.1:p.Asn410Lys
ENST00000698871.1:n.1753C>G
ENST00000698872.1:c.*19C>G	ENSP00000513997.1:n.*19C>G
ENST00000698873.1:c.*425C>G	ENSP00000513998.1:n.*425C>G
ENST00000698874.1:c.690C>G	ENSP00000513999.1:p.Asn230Lys
ENST00000698875.1:n.1090C>G
ENST00000698876.1:n.1169C>G
ENST00000698877.1:n.798C>G
ENST00000698878.1:c.1230C>G	ENSP00000514000.1:p.Asn410Lys
ENST00000698880.1:c.1070C>G
ENST00000345728.10:c.1230C>G MANE Select	ENSP00000339950.5:p.Asn410Lys
ENST00000279227.9:c.1242C>G	ENSP00000279227.5:p.Asn414Lys
ENST00000345728.9:c.1230C>G	ENSP00000339950.5:p.Asn410Lys
ENST00000540957.1:n.383C>G
ENST00000541326.5:n.537C>G
NM_031471.5:c.1230C>G	NP_113659.3:p.Asn410Lys
NM_178443.2:c.1242C>G , LRG_180t1:c.1242C>G	NP_848537.1:p.Asn414Lys
XM_011545294.1:c.1242C>G	XP_011543596.1:p.Asn414Lys
XM_011545295.1:c.702C>G	XP_011543597.1:p.Asn234Lys
XM_011545296.1:c.702C>G	XP_011543598.1:p.Asn234Lys
XM_011545294.3:c.1242C>G	XP_011543596.1:p.Asn414Lys
XM_011545295.2:c.702C>G	XP_011543597.1:p.Asn234Lys
XM_017018398.2:c.1230C>G	XP_016873887.1:p.Asn410Lys
XM_017018399.1:c.690C>G	XP_016873888.1:p.Asn230Lys
NM_031471.6:c.1230C>G MANE Select	NP_113659.3:p.Asn410Lys
NM_001382361.1:c.1230C>G	NP_001369290.1:p.Asn410Lys
NM_001382362.1:c.1242C>G	NP_001369291.1:p.Asn414Lys
NM_001382363.1:c.690C>G	NP_001369292.1:p.Asn230Lys
NM_001382364.1:c.702C>G	NP_001369293.1:p.Asn234Lys
NM_001382448.1:c.1230C>G	NP_001369377.1:p.Asn410Lys
NM_178443.3:c.1242C>G	NP_848537.1:p.Asn414Lys