Canonical Allele Identifier: CA381090075

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990640T>G (hg19) ; chr11:g.64223168T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223168T>G , CM000673.2:g.64223168T>G	GRCh38
NC_000011.9:g.63990640T>G , CM000673.1:g.63990640T>G	GRCh37
NC_000011.8:g.63747216T>G	NCBI36
NG_016360.1:g.21489T>G , LRG_180:g.21489T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1803T>G	ENSP00000279227.5:p.Asn601Lys
ENST00000540554.2:n.3315T>G
ENST00000541252.2:c.1251T>G	ENSP00000438885.2:p.Asn417Lys
ENST00000544997.6:c.1791T>G	ENSP00000445778.2:p.Asn597Lys
ENST00000545896.2:c.355T>G	ENSP00000440209.2:p.Cys119Gly
ENST00000546255.2:n.2095T>G
ENST00000698845.1:c.*986T>G	ENSP00000513981.1:n.*986T>G
ENST00000698846.1:n.2037T>G
ENST00000698847.1:c.*1196T>G	ENSP00000513982.1:n.*1196T>G
ENST00000698850.1:n.3812T>G
ENST00000698852.1:c.1791T>G	ENSP00000513984.1:p.Asn597Lys
ENST00000698853.1:c.*1020T>G	ENSP00000513985.1:n.*1020T>G
ENST00000698854.1:c.*1121T>G	ENSP00000513986.1:n.*1121T>G
ENST00000698855.1:n.3443T>G
ENST00000698856.1:n.3137T>G
ENST00000698859.1:n.2301T>G
ENST00000698860.1:c.1803T>G	ENSP00000513988.1:p.Asn601Lys
ENST00000698861.1:c.1791T>G	ENSP00000513989.1:p.Asn597Lys
ENST00000698862.1:c.*1087T>G	ENSP00000513990.1:n.*1087T>G
ENST00000698863.1:c.1791T>G	ENSP00000513991.1:p.Asn597Lys
ENST00000698864.1:n.2352T>G
ENST00000698865.1:c.1812T>G	ENSP00000513992.1:p.Asn604Lys
ENST00000698866.1:c.*1579T>G	ENSP00000513993.1:n.*1579T>G
ENST00000698867.1:n.5766T>G
ENST00000698868.1:c.1656T>G	ENSP00000513994.1:p.Asn552Lys
ENST00000698869.1:c.1557T>G	ENSP00000513995.1:p.Asn519Lys
ENST00000698870.1:c.1791T>G	ENSP00000513996.1:p.Asn597Lys
ENST00000698871.1:n.2314T>G
ENST00000698872.1:c.*580T>G	ENSP00000513997.1:n.*580T>G
ENST00000698873.1:c.*986T>G	ENSP00000513998.1:n.*986T>G
ENST00000698874.1:c.1251T>G	ENSP00000513999.1:p.Asn417Lys
ENST00000698875.1:n.1651T>G
ENST00000698876.1:n.1839T>G
ENST00000698877.1:n.1359T>G
ENST00000698878.1:c.1785T>G	ENSP00000514000.1:p.Asn595Lys
ENST00000698880.1:c.1659T>G
ENST00000345728.10:c.1791T>G MANE Select	ENSP00000339950.5:p.Asn597Lys
ENST00000279227.9:c.1803T>G	ENSP00000279227.5:p.Asn601Lys
ENST00000345728.9:c.1791T>G	ENSP00000339950.5:p.Asn597Lys
ENST00000545896.1:c.354T>G	ENSP00000440209.1:p.Asn118Lys
NM_031471.5:c.1791T>G	NP_113659.3:p.Asn597Lys
NM_178443.2:c.1803T>G , LRG_180t1:c.1803T>G	NP_848537.1:p.Asn601Lys
XM_011545294.1:c.1803T>G	XP_011543596.1:p.Asn601Lys
XM_011545295.1:c.1263T>G	XP_011543597.1:p.Asn421Lys
XM_011545296.1:c.1263T>G	XP_011543598.1:p.Asn421Lys
XM_011545294.3:c.1803T>G	XP_011543596.1:p.Asn601Lys
XM_011545295.2:c.1263T>G	XP_011543597.1:p.Asn421Lys
XM_017018398.2:c.1791T>G	XP_016873887.1:p.Asn597Lys
XM_017018399.1:c.1251T>G	XP_016873888.1:p.Asn417Lys
NM_031471.6:c.1791T>G MANE Select	NP_113659.3:p.Asn597Lys
NM_001382361.1:c.1791T>G	NP_001369290.1:p.Asn597Lys
NM_001382362.1:c.1803T>G	NP_001369291.1:p.Asn601Lys
NM_001382363.1:c.1251T>G	NP_001369292.1:p.Asn417Lys
NM_001382364.1:c.1263T>G	NP_001369293.1:p.Asn421Lys
NM_001382448.1:c.1791T>G	NP_001369377.1:p.Asn597Lys
NM_178443.3:c.1803T>G	NP_848537.1:p.Asn601Lys