Canonical Allele Identifier: CA381090150

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990653A>C (hg19) ; chr11:g.64223181A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223181A>C , CM000673.2:g.64223181A>C	GRCh38
NC_000011.9:g.63990653A>C , CM000673.1:g.63990653A>C	GRCh37
NC_000011.8:g.63747229A>C	NCBI36
NG_016360.1:g.21502A>C , LRG_180:g.21502A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1816A>C	ENSP00000279227.5:p.Ile606Leu
ENST00000540554.2:n.3328A>C
ENST00000541252.2:c.1264A>C	ENSP00000438885.2:p.Ile422Leu
ENST00000544997.6:c.1804A>C	ENSP00000445778.2:p.Ile602Leu
ENST00000545896.2:c.368A>C	ENSP00000440209.2:p.His123Pro
ENST00000546255.2:n.2108A>C
ENST00000698845.1:c.*999A>C	ENSP00000513981.1:n.*999A>C
ENST00000698846.1:n.2050A>C
ENST00000698847.1:c.*1209A>C	ENSP00000513982.1:n.*1209A>C
ENST00000698850.1:n.3825A>C
ENST00000698852.1:c.1804A>C	ENSP00000513984.1:p.Ile602Leu
ENST00000698853.1:c.*1033A>C	ENSP00000513985.1:n.*1033A>C
ENST00000698854.1:c.*1134A>C	ENSP00000513986.1:n.*1134A>C
ENST00000698855.1:n.3456A>C
ENST00000698856.1:n.3150A>C
ENST00000698859.1:n.2314A>C
ENST00000698860.1:c.1816A>C	ENSP00000513988.1:p.Ile606Leu
ENST00000698861.1:c.1804A>C	ENSP00000513989.1:p.Ile602Leu
ENST00000698862.1:c.*1100A>C	ENSP00000513990.1:n.*1100A>C
ENST00000698863.1:c.1804A>C	ENSP00000513991.1:p.Ile602Leu
ENST00000698864.1:n.2365A>C
ENST00000698865.1:c.1825A>C	ENSP00000513992.1:p.Ile609Leu
ENST00000698866.1:c.*1592A>C	ENSP00000513993.1:n.*1592A>C
ENST00000698867.1:n.5779A>C
ENST00000698868.1:c.1669A>C	ENSP00000513994.1:p.Ile557Leu
ENST00000698869.1:c.1570A>C	ENSP00000513995.1:p.Ile524Leu
ENST00000698870.1:c.1804A>C	ENSP00000513996.1:p.Ile602Leu
ENST00000698871.1:n.2327A>C
ENST00000698872.1:c.*593A>C	ENSP00000513997.1:n.*593A>C
ENST00000698873.1:c.*999A>C	ENSP00000513998.1:n.*999A>C
ENST00000698874.1:c.1264A>C	ENSP00000513999.1:p.Ile422Leu
ENST00000698875.1:n.1664A>C
ENST00000698876.1:n.1852A>C
ENST00000698877.1:n.1372A>C
ENST00000698878.1:c.1798A>C	ENSP00000514000.1:p.Ile600Leu
ENST00000698880.1:c.1672A>C
ENST00000345728.10:c.1804A>C MANE Select	ENSP00000339950.5:p.Ile602Leu
ENST00000279227.9:c.1816A>C	ENSP00000279227.5:p.Ile606Leu
ENST00000345728.9:c.1804A>C	ENSP00000339950.5:p.Ile602Leu
ENST00000545896.1:c.367A>C	ENSP00000440209.1:p.Ile123Leu
NM_031471.5:c.1804A>C	NP_113659.3:p.Ile602Leu
NM_178443.2:c.1816A>C , LRG_180t1:c.1816A>C	NP_848537.1:p.Ile606Leu
XM_011545294.1:c.1816A>C	XP_011543596.1:p.Ile606Leu
XM_011545295.1:c.1276A>C	XP_011543597.1:p.Ile426Leu
XM_011545296.1:c.1276A>C	XP_011543598.1:p.Ile426Leu
XM_011545294.3:c.1816A>C	XP_011543596.1:p.Ile606Leu
XM_011545295.2:c.1276A>C	XP_011543597.1:p.Ile426Leu
XM_017018398.2:c.1804A>C	XP_016873887.1:p.Ile602Leu
XM_017018399.1:c.1264A>C	XP_016873888.1:p.Ile422Leu
NM_031471.6:c.1804A>C MANE Select	NP_113659.3:p.Ile602Leu
NM_001382361.1:c.1804A>C	NP_001369290.1:p.Ile602Leu
NM_001382362.1:c.1816A>C	NP_001369291.1:p.Ile606Leu
NM_001382363.1:c.1264A>C	NP_001369292.1:p.Ile422Leu
NM_001382364.1:c.1276A>C	NP_001369293.1:p.Ile426Leu
NM_001382448.1:c.1804A>C	NP_001369377.1:p.Ile602Leu
NM_178443.3:c.1816A>C	NP_848537.1:p.Ile606Leu