Canonical Allele Identifier: CA475151712

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987705T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220233T>C , CM000673.2:g.64220233T>C	GRCh38
NC_000011.9:g.63987705T>C , CM000673.1:g.63987705T>C	GRCh37
NC_000011.8:g.63744281T>C	NCBI36
NG_016360.1:g.18554T>C , LRG_180:g.18554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1230T>C	ENSP00000279227.5:p.Val410=
ENST00000540554.2:n.2287T>C
ENST00000541252.2:c.678T>C	ENSP00000438885.2:p.Val226=
ENST00000541326.6:n.530T>C
ENST00000544997.6:c.1218T>C	ENSP00000445778.2:p.Val406=
ENST00000546255.2:n.1413T>C
ENST00000698845.1:c.*413T>C	ENSP00000513981.1:n.*413T>C
ENST00000698846.1:n.1355T>C
ENST00000698847.1:c.*623T>C	ENSP00000513982.1:n.*623T>C
ENST00000698848.1:n.407T>C
ENST00000698849.1:n.338T>C
ENST00000698850.1:n.877T>C
ENST00000698852.1:c.1218T>C	ENSP00000513984.1:p.Val406=
ENST00000698853.1:c.*447T>C	ENSP00000513985.1:n.*447T>C
ENST00000698854.1:c.*548T>C	ENSP00000513986.1:n.*548T>C
ENST00000698855.1:n.2870T>C
ENST00000698856.1:n.2455T>C
ENST00000698859.1:n.1382T>C
ENST00000698860.1:c.1230T>C	ENSP00000513988.1:p.Val410=
ENST00000698861.1:c.1218T>C	ENSP00000513989.1:p.Val406=
ENST00000698862.1:c.*514T>C	ENSP00000513990.1:n.*514T>C
ENST00000698863.1:c.1218T>C	ENSP00000513991.1:p.Val406=
ENST00000698864.1:n.1324T>C
ENST00000698865.1:c.1239T>C	ENSP00000513992.1:p.Val413=
ENST00000698866.1:c.*623T>C	ENSP00000513993.1:n.*623T>C
ENST00000698867.1:n.5193T>C
ENST00000698868.1:c.1083T>C	ENSP00000513994.1:p.Val361=
ENST00000698869.1:c.1218T>C	ENSP00000513995.1:p.Val406=
ENST00000698870.1:c.1218T>C	ENSP00000513996.1:p.Val406=
ENST00000698871.1:n.1741T>C
ENST00000698872.1:c.*7T>C	ENSP00000513997.1:n.*7T>C
ENST00000698873.1:c.*413T>C	ENSP00000513998.1:n.*413T>C
ENST00000698874.1:c.678T>C	ENSP00000513999.1:p.Val226=
ENST00000698875.1:n.1078T>C
ENST00000698876.1:n.1157T>C
ENST00000698877.1:n.786T>C
ENST00000698878.1:c.1218T>C	ENSP00000514000.1:p.Val406=
ENST00000698880.1:c.1058T>C
ENST00000345728.10:c.1218T>C MANE Select	ENSP00000339950.5:p.Val406=
ENST00000279227.9:c.1230T>C	ENSP00000279227.5:p.Val410=
ENST00000345728.9:c.1218T>C	ENSP00000339950.5:p.Val406=
ENST00000540957.1:n.371T>C
ENST00000541326.5:n.525T>C
NM_031471.5:c.1218T>C	NP_113659.3:p.Val406=
NM_178443.2:c.1230T>C , LRG_180t1:c.1230T>C	NP_848537.1:p.Val410=
XM_011545294.1:c.1230T>C	XP_011543596.1:p.Val410=
XM_011545295.1:c.690T>C	XP_011543597.1:p.Val230=
XM_011545296.1:c.690T>C	XP_011543598.1:p.Val230=
XM_011545294.3:c.1230T>C	XP_011543596.1:p.Val410=
XM_011545295.2:c.690T>C	XP_011543597.1:p.Val230=
XM_017018398.2:c.1218T>C	XP_016873887.1:p.Val406=
XM_017018399.1:c.678T>C	XP_016873888.1:p.Val226=
NM_031471.6:c.1218T>C MANE Select	NP_113659.3:p.Val406=
NM_001382361.1:c.1218T>C	NP_001369290.1:p.Val406=
NM_001382362.1:c.1230T>C	NP_001369291.1:p.Val410=
NM_001382363.1:c.678T>C	NP_001369292.1:p.Val226=
NM_001382364.1:c.690T>C	NP_001369293.1:p.Val230=
NM_001382448.1:c.1218T>C	NP_001369377.1:p.Val406=
NM_178443.3:c.1230T>C	NP_848537.1:p.Val410=