Canonical Allele Identifier: CA381087126

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987752T>G (hg19) ; chr11:g.64220280T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220280T>G , CM000673.2:g.64220280T>G	GRCh38
NC_000011.9:g.63987752T>G , CM000673.1:g.63987752T>G	GRCh37
NC_000011.8:g.63744328T>G	NCBI36
NG_016360.1:g.18601T>G , LRG_180:g.18601T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1277T>G	ENSP00000279227.5:p.Val426Gly
ENST00000540554.2:n.2334T>G
ENST00000541252.2:c.725T>G	ENSP00000438885.2:p.Val242Gly
ENST00000541326.6:n.577T>G
ENST00000544997.6:c.1265T>G	ENSP00000445778.2:p.Val422Gly
ENST00000546255.2:n.1460T>G
ENST00000698845.1:c.*460T>G	ENSP00000513981.1:n.*460T>G
ENST00000698846.1:n.1402T>G
ENST00000698847.1:c.*670T>G	ENSP00000513982.1:n.*670T>G
ENST00000698848.1:n.454T>G
ENST00000698849.1:n.385T>G
ENST00000698850.1:n.924T>G
ENST00000698852.1:c.1265T>G	ENSP00000513984.1:p.Val422Gly
ENST00000698853.1:c.*494T>G	ENSP00000513985.1:n.*494T>G
ENST00000698854.1:c.*595T>G	ENSP00000513986.1:n.*595T>G
ENST00000698855.1:n.2917T>G
ENST00000698856.1:n.2502T>G
ENST00000698859.1:n.1429T>G
ENST00000698860.1:c.1277T>G	ENSP00000513988.1:p.Val426Gly
ENST00000698861.1:c.1265T>G	ENSP00000513989.1:p.Val422Gly
ENST00000698862.1:c.*561T>G	ENSP00000513990.1:n.*561T>G
ENST00000698863.1:c.1265T>G	ENSP00000513991.1:p.Val422Gly
ENST00000698864.1:n.1371T>G
ENST00000698865.1:c.1286T>G	ENSP00000513992.1:p.Val429Gly
ENST00000698866.1:c.*670T>G	ENSP00000513993.1:n.*670T>G
ENST00000698867.1:n.5240T>G
ENST00000698868.1:c.1130T>G	ENSP00000513994.1:p.Val377Gly
ENST00000698869.1:c.1265T>G	ENSP00000513995.1:p.Val422Gly
ENST00000698870.1:c.1265T>G	ENSP00000513996.1:p.Val422Gly
ENST00000698871.1:n.1788T>G
ENST00000698872.1:c.*54T>G	ENSP00000513997.1:n.*54T>G
ENST00000698873.1:c.*460T>G	ENSP00000513998.1:n.*460T>G
ENST00000698874.1:c.725T>G	ENSP00000513999.1:p.Val242Gly
ENST00000698875.1:n.1125T>G
ENST00000698876.1:n.1204T>G
ENST00000698877.1:n.833T>G
ENST00000698878.1:c.1265T>G	ENSP00000514000.1:p.Val422Gly
ENST00000698880.1:c.1105T>G
ENST00000345728.10:c.1265T>G MANE Select	ENSP00000339950.5:p.Val422Gly
ENST00000279227.9:c.1277T>G	ENSP00000279227.5:p.Val426Gly
ENST00000345728.9:c.1265T>G	ENSP00000339950.5:p.Val422Gly
ENST00000540957.1:n.418T>G
ENST00000541326.5:n.572T>G
NM_031471.5:c.1265T>G	NP_113659.3:p.Val422Gly
NM_178443.2:c.1277T>G , LRG_180t1:c.1277T>G	NP_848537.1:p.Val426Gly
XM_011545294.1:c.1277T>G	XP_011543596.1:p.Val426Gly
XM_011545295.1:c.737T>G	XP_011543597.1:p.Val246Gly
XM_011545296.1:c.737T>G	XP_011543598.1:p.Val246Gly
XM_011545294.3:c.1277T>G	XP_011543596.1:p.Val426Gly
XM_011545295.2:c.737T>G	XP_011543597.1:p.Val246Gly
XM_017018398.2:c.1265T>G	XP_016873887.1:p.Val422Gly
XM_017018399.1:c.725T>G	XP_016873888.1:p.Val242Gly
NM_031471.6:c.1265T>G MANE Select	NP_113659.3:p.Val422Gly
NM_001382361.1:c.1265T>G	NP_001369290.1:p.Val422Gly
NM_001382362.1:c.1277T>G	NP_001369291.1:p.Val426Gly
NM_001382363.1:c.725T>G	NP_001369292.1:p.Val242Gly
NM_001382364.1:c.737T>G	NP_001369293.1:p.Val246Gly
NM_001382448.1:c.1265T>G	NP_001369377.1:p.Val422Gly
NM_178443.3:c.1277T>G	NP_848537.1:p.Val426Gly