Canonical Allele Identifier: CA381087182

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64220298-T-C
• MyVariant Identifiers: chr11:g.63987770T>C (hg19) ; chr11:g.64220298T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220298T>C , CM000673.2:g.64220298T>C	GRCh38
NC_000011.9:g.63987770T>C , CM000673.1:g.63987770T>C	GRCh37
NC_000011.8:g.63744346T>C	NCBI36
NG_016360.1:g.18619T>C , LRG_180:g.18619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1295T>C	ENSP00000279227.5:p.Met432Thr
ENST00000540554.2:n.2352T>C
ENST00000541252.2:c.743T>C	ENSP00000438885.2:p.Met248Thr
ENST00000541326.6:n.595T>C
ENST00000544997.6:c.1283T>C	ENSP00000445778.2:p.Met428Thr
ENST00000546255.2:n.1478T>C
ENST00000698845.1:c.*478T>C	ENSP00000513981.1:n.*478T>C
ENST00000698846.1:n.1420T>C
ENST00000698847.1:c.*688T>C	ENSP00000513982.1:n.*688T>C
ENST00000698848.1:n.472T>C
ENST00000698849.1:n.403T>C
ENST00000698850.1:n.942T>C
ENST00000698852.1:c.1283T>C	ENSP00000513984.1:p.Met428Thr
ENST00000698853.1:c.*512T>C	ENSP00000513985.1:n.*512T>C
ENST00000698854.1:c.*613T>C	ENSP00000513986.1:n.*613T>C
ENST00000698855.1:n.2935T>C
ENST00000698856.1:n.2520T>C
ENST00000698859.1:n.1447T>C
ENST00000698860.1:c.1295T>C	ENSP00000513988.1:p.Met432Thr
ENST00000698861.1:c.1283T>C	ENSP00000513989.1:p.Met428Thr
ENST00000698862.1:c.*579T>C	ENSP00000513990.1:n.*579T>C
ENST00000698863.1:c.1283T>C	ENSP00000513991.1:p.Met428Thr
ENST00000698864.1:n.1389T>C
ENST00000698865.1:c.1304T>C	ENSP00000513992.1:p.Met435Thr
ENST00000698866.1:c.*688T>C	ENSP00000513993.1:n.*688T>C
ENST00000698867.1:n.5258T>C
ENST00000698868.1:c.1148T>C	ENSP00000513994.1:p.Met383Thr
ENST00000698869.1:c.1283T>C	ENSP00000513995.1:p.Met428Thr
ENST00000698870.1:c.1283T>C	ENSP00000513996.1:p.Met428Thr
ENST00000698871.1:n.1806T>C
ENST00000698872.1:c.*72T>C	ENSP00000513997.1:n.*72T>C
ENST00000698873.1:c.*478T>C	ENSP00000513998.1:n.*478T>C
ENST00000698874.1:c.743T>C	ENSP00000513999.1:p.Met248Thr
ENST00000698875.1:n.1143T>C
ENST00000698876.1:n.1222T>C
ENST00000698877.1:n.851T>C
ENST00000698878.1:c.1283T>C	ENSP00000514000.1:p.Met428Thr
ENST00000698880.1:c.1123T>C
ENST00000345728.10:c.1283T>C MANE Select	ENSP00000339950.5:p.Met428Thr
ENST00000279227.9:c.1295T>C	ENSP00000279227.5:p.Met432Thr
ENST00000345728.9:c.1283T>C	ENSP00000339950.5:p.Met428Thr
ENST00000540957.1:n.436T>C
ENST00000541326.5:n.590T>C
NM_031471.5:c.1283T>C	NP_113659.3:p.Met428Thr
NM_178443.2:c.1295T>C , LRG_180t1:c.1295T>C	NP_848537.1:p.Met432Thr
XM_011545294.1:c.1295T>C	XP_011543596.1:p.Met432Thr
XM_011545295.1:c.755T>C	XP_011543597.1:p.Met252Thr
XM_011545296.1:c.755T>C	XP_011543598.1:p.Met252Thr
XM_011545294.3:c.1295T>C	XP_011543596.1:p.Met432Thr
XM_011545295.2:c.755T>C	XP_011543597.1:p.Met252Thr
XM_017018398.2:c.1283T>C	XP_016873887.1:p.Met428Thr
XM_017018399.1:c.743T>C	XP_016873888.1:p.Met248Thr
NM_031471.6:c.1283T>C MANE Select	NP_113659.3:p.Met428Thr
NM_001382361.1:c.1283T>C	NP_001369290.1:p.Met428Thr
NM_001382362.1:c.1295T>C	NP_001369291.1:p.Met432Thr
NM_001382363.1:c.743T>C	NP_001369292.1:p.Met248Thr
NM_001382364.1:c.755T>C	NP_001369293.1:p.Met252Thr
NM_001382448.1:c.1283T>C	NP_001369377.1:p.Met428Thr
NM_178443.3:c.1295T>C	NP_848537.1:p.Met432Thr