Canonical Allele Identifier: CA381089745

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63990581G>C (hg19) ; chr11:g.64223109G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223109G>C , CM000673.2:g.64223109G>C	GRCh38
NC_000011.9:g.63990581G>C , CM000673.1:g.63990581G>C	GRCh37
NC_000011.8:g.63747157G>C	NCBI36
NG_016360.1:g.21430G>C , LRG_180:g.21430G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1744G>C	ENSP00000279227.5:p.Asp582His
ENST00000540554.2:n.3256G>C
ENST00000541252.2:c.1192G>C	ENSP00000438885.2:p.Asp398His
ENST00000544997.6:c.1732G>C	ENSP00000445778.2:p.Asp578His
ENST00000545896.2:c.296G>C	ENSP00000440209.2:p.Arg99Pro
ENST00000546255.2:n.2036G>C
ENST00000698845.1:c.*927G>C	ENSP00000513981.1:n.*927G>C
ENST00000698846.1:n.1978G>C
ENST00000698847.1:c.*1137G>C	ENSP00000513982.1:n.*1137G>C
ENST00000698850.1:n.3753G>C
ENST00000698852.1:c.1732G>C	ENSP00000513984.1:p.Asp578His
ENST00000698853.1:c.*961G>C	ENSP00000513985.1:n.*961G>C
ENST00000698854.1:c.*1062G>C	ENSP00000513986.1:n.*1062G>C
ENST00000698855.1:n.3384G>C
ENST00000698856.1:n.3078G>C
ENST00000698859.1:n.2242G>C
ENST00000698860.1:c.1744G>C	ENSP00000513988.1:p.Asp582His
ENST00000698861.1:c.1732G>C	ENSP00000513989.1:p.Asp578His
ENST00000698862.1:c.*1028G>C	ENSP00000513990.1:n.*1028G>C
ENST00000698863.1:c.1732G>C	ENSP00000513991.1:p.Asp578His
ENST00000698864.1:n.2293G>C
ENST00000698865.1:c.1753G>C	ENSP00000513992.1:p.Asp585His
ENST00000698866.1:c.*1520G>C	ENSP00000513993.1:n.*1520G>C
ENST00000698867.1:n.5707G>C
ENST00000698868.1:c.1597G>C	ENSP00000513994.1:p.Asp533His
ENST00000698869.1:c.1498G>C	ENSP00000513995.1:p.Asp500His
ENST00000698870.1:c.1732G>C	ENSP00000513996.1:p.Asp578His
ENST00000698871.1:n.2255G>C
ENST00000698872.1:c.*521G>C	ENSP00000513997.1:n.*521G>C
ENST00000698873.1:c.*927G>C	ENSP00000513998.1:n.*927G>C
ENST00000698874.1:c.1192G>C	ENSP00000513999.1:p.Asp398His
ENST00000698875.1:n.1592G>C
ENST00000698876.1:n.1780G>C
ENST00000698877.1:n.1300G>C
ENST00000698878.1:c.1726G>C	ENSP00000514000.1:p.Asp576His
ENST00000698880.1:c.1600G>C
ENST00000345728.10:c.1732G>C MANE Select	ENSP00000339950.5:p.Asp578His
ENST00000279227.9:c.1744G>C	ENSP00000279227.5:p.Asp582His
ENST00000345728.9:c.1732G>C	ENSP00000339950.5:p.Asp578His
ENST00000540554.1:n.368G>C
ENST00000545896.1:c.295G>C	ENSP00000440209.1:p.Asp99His
NM_031471.5:c.1732G>C	NP_113659.3:p.Asp578His
NM_178443.2:c.1744G>C , LRG_180t1:c.1744G>C	NP_848537.1:p.Asp582His
XM_011545294.1:c.1744G>C	XP_011543596.1:p.Asp582His
XM_011545295.1:c.1204G>C	XP_011543597.1:p.Asp402His
XM_011545296.1:c.1204G>C	XP_011543598.1:p.Asp402His
XM_011545294.3:c.1744G>C	XP_011543596.1:p.Asp582His
XM_011545295.2:c.1204G>C	XP_011543597.1:p.Asp402His
XM_017018398.2:c.1732G>C	XP_016873887.1:p.Asp578His
XM_017018399.1:c.1192G>C	XP_016873888.1:p.Asp398His
NM_031471.6:c.1732G>C MANE Select	NP_113659.3:p.Asp578His
NM_001382361.1:c.1732G>C	NP_001369290.1:p.Asp578His
NM_001382362.1:c.1744G>C	NP_001369291.1:p.Asp582His
NM_001382363.1:c.1192G>C	NP_001369292.1:p.Asp398His
NM_001382364.1:c.1204G>C	NP_001369293.1:p.Asp402His
NM_001382448.1:c.1732G>C	NP_001369377.1:p.Asp578His
NM_178443.3:c.1744G>C	NP_848537.1:p.Asp582His