Canonical Allele Identifier: CA381087867

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988036T>C (hg19) ; chr11:g.64220564T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220564T>C , CM000673.2:g.64220564T>C	GRCh38
NC_000011.9:g.63988036T>C , CM000673.1:g.63988036T>C	GRCh37
NC_000011.8:g.63744612T>C	NCBI36
NG_016360.1:g.18885T>C , LRG_180:g.18885T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1452T>C	ENSP00000279227.5:p.Ser484=
ENST00000540554.2:n.2618T>C
ENST00000541252.2:c.900T>C	ENSP00000438885.2:p.Ser300=
ENST00000541326.6:n.861T>C
ENST00000544997.6:c.1440T>C	ENSP00000445778.2:p.Ser480=
ENST00000545896.2:c.129T>C	ENSP00000440209.2:p.Ser43=
ENST00000546255.2:n.1744T>C
ENST00000698845.1:c.*635T>C	ENSP00000513981.1:n.*635T>C
ENST00000698846.1:n.1686T>C
ENST00000698847.1:c.*845T>C	ENSP00000513982.1:n.*845T>C
ENST00000698849.1:n.560T>C
ENST00000698850.1:n.1208T>C
ENST00000698852.1:c.1440T>C	ENSP00000513984.1:p.Ser480=
ENST00000698853.1:c.*669T>C	ENSP00000513985.1:n.*669T>C
ENST00000698854.1:c.*770T>C	ENSP00000513986.1:n.*770T>C
ENST00000698855.1:n.3092T>C
ENST00000698856.1:n.2786T>C
ENST00000698859.1:n.1604T>C
ENST00000698860.1:c.1452T>C	ENSP00000513988.1:p.Ser484=
ENST00000698861.1:c.1440T>C	ENSP00000513989.1:p.Ser480=
ENST00000698862.1:c.*736T>C	ENSP00000513990.1:n.*736T>C
ENST00000698863.1:c.1440T>C	ENSP00000513991.1:p.Ser480=
ENST00000698864.1:n.1655T>C
ENST00000698865.1:c.1461T>C	ENSP00000513992.1:p.Ser487=
ENST00000698866.1:c.*954T>C	ENSP00000513993.1:n.*954T>C
ENST00000698867.1:n.5415T>C
ENST00000698868.1:c.1305T>C	ENSP00000513994.1:p.Ser435=
ENST00000698869.1:c.1311+238T>C	ENSP00000513995.1:n.1311+238T>C
ENST00000698870.1:c.1440T>C	ENSP00000513996.1:p.Ser480=
ENST00000698871.1:n.1963T>C
ENST00000698872.1:c.*229T>C	ENSP00000513997.1:n.*229T>C
ENST00000698873.1:c.*635T>C	ENSP00000513998.1:n.*635T>C
ENST00000698874.1:c.900T>C	ENSP00000513999.1:p.Ser300=
ENST00000698875.1:n.1300T>C
ENST00000698876.1:n.1488T>C
ENST00000698877.1:n.1008T>C
ENST00000698878.1:c.1434T>C	ENSP00000514000.1:p.Ser478=
ENST00000698880.1:c.1308T>C
ENST00000345728.10:c.1440T>C MANE Select	ENSP00000339950.5:p.Ser480=
ENST00000279227.9:c.1452T>C	ENSP00000279227.5:p.Ser484=
ENST00000345728.9:c.1440T>C	ENSP00000339950.5:p.Ser480=
ENST00000541326.5:n.856T>C
ENST00000545896.1:c.128T>C	ENSP00000440209.1:p.Val43Ala
NM_031471.5:c.1440T>C	NP_113659.3:p.Ser480=
NM_178443.2:c.1452T>C , LRG_180t1:c.1452T>C	NP_848537.1:p.Ser484=
XM_011545294.1:c.1452T>C	XP_011543596.1:p.Ser484=
XM_011545295.1:c.912T>C	XP_011543597.1:p.Ser304=
XM_011545296.1:c.912T>C	XP_011543598.1:p.Ser304=
XM_011545294.3:c.1452T>C	XP_011543596.1:p.Ser484=
XM_011545295.2:c.912T>C	XP_011543597.1:p.Ser304=
XM_017018398.2:c.1440T>C	XP_016873887.1:p.Ser480=
XM_017018399.1:c.900T>C	XP_016873888.1:p.Ser300=
NM_031471.6:c.1440T>C MANE Select	NP_113659.3:p.Ser480=
NM_001382361.1:c.1440T>C	NP_001369290.1:p.Ser480=
NM_001382362.1:c.1452T>C	NP_001369291.1:p.Ser484=
NM_001382363.1:c.900T>C	NP_001369292.1:p.Ser300=
NM_001382364.1:c.912T>C	NP_001369293.1:p.Ser304=
NM_001382448.1:c.1440T>C	NP_001369377.1:p.Ser480=
NM_178443.3:c.1452T>C	NP_848537.1:p.Ser484=