Canonical Allele Identifier: CA381087421

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987930T>C (hg19) ; chr11:g.64220458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220458T>C , CM000673.2:g.64220458T>C	GRCh38
NC_000011.9:g.63987930T>C , CM000673.1:g.63987930T>C	GRCh37
NC_000011.8:g.63744506T>C	NCBI36
NG_016360.1:g.18779T>C , LRG_180:g.18779T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1346T>C	ENSP00000279227.5:p.Met449Thr
ENST00000540554.2:n.2512T>C
ENST00000541252.2:c.794T>C	ENSP00000438885.2:p.Met265Thr
ENST00000541326.6:n.755T>C
ENST00000544997.6:c.1334T>C	ENSP00000445778.2:p.Met445Thr
ENST00000545896.2:c.23T>C	ENSP00000440209.2:p.Met8Thr
ENST00000546255.2:n.1638T>C
ENST00000698845.1:c.*529T>C	ENSP00000513981.1:n.*529T>C
ENST00000698846.1:n.1580T>C
ENST00000698847.1:c.*739T>C	ENSP00000513982.1:n.*739T>C
ENST00000698848.1:n.632T>C
ENST00000698849.1:n.454T>C
ENST00000698850.1:n.1102T>C
ENST00000698852.1:c.1334T>C	ENSP00000513984.1:p.Met445Thr
ENST00000698853.1:c.*563T>C	ENSP00000513985.1:n.*563T>C
ENST00000698854.1:c.*664T>C	ENSP00000513986.1:n.*664T>C
ENST00000698855.1:n.2986T>C
ENST00000698856.1:n.2680T>C
ENST00000698859.1:n.1498T>C
ENST00000698860.1:c.1346T>C	ENSP00000513988.1:p.Met449Thr
ENST00000698861.1:c.1334T>C	ENSP00000513989.1:p.Met445Thr
ENST00000698862.1:c.*630T>C	ENSP00000513990.1:n.*630T>C
ENST00000698863.1:c.1334T>C	ENSP00000513991.1:p.Met445Thr
ENST00000698864.1:n.1549T>C
ENST00000698865.1:c.1355T>C	ENSP00000513992.1:p.Met452Thr
ENST00000698866.1:c.*848T>C	ENSP00000513993.1:n.*848T>C
ENST00000698867.1:n.5309T>C
ENST00000698868.1:c.1199T>C	ENSP00000513994.1:p.Met400Thr
ENST00000698869.1:c.1311+132T>C	ENSP00000513995.1:n.1311+132T>C
ENST00000698870.1:c.1334T>C	ENSP00000513996.1:p.Met445Thr
ENST00000698871.1:n.1857T>C
ENST00000698872.1:c.*123T>C	ENSP00000513997.1:n.*123T>C
ENST00000698873.1:c.*529T>C	ENSP00000513998.1:n.*529T>C
ENST00000698874.1:c.794T>C	ENSP00000513999.1:p.Met265Thr
ENST00000698875.1:n.1194T>C
ENST00000698876.1:n.1382T>C
ENST00000698877.1:n.902T>C
ENST00000698878.1:c.1328T>C	ENSP00000514000.1:p.Met443Thr
ENST00000698880.1:c.1202T>C
ENST00000345728.10:c.1334T>C MANE Select	ENSP00000339950.5:p.Met445Thr
ENST00000279227.9:c.1346T>C	ENSP00000279227.5:p.Met449Thr
ENST00000345728.9:c.1334T>C	ENSP00000339950.5:p.Met445Thr
ENST00000541326.5:n.750T>C
ENST00000545896.1:c.22T>C	ENSP00000440209.1:p.Trp8Arg
NM_031471.5:c.1334T>C	NP_113659.3:p.Met445Thr
NM_178443.2:c.1346T>C , LRG_180t1:c.1346T>C	NP_848537.1:p.Met449Thr
XM_011545294.1:c.1346T>C	XP_011543596.1:p.Met449Thr
XM_011545295.1:c.806T>C	XP_011543597.1:p.Met269Thr
XM_011545296.1:c.806T>C	XP_011543598.1:p.Met269Thr
XM_011545294.3:c.1346T>C	XP_011543596.1:p.Met449Thr
XM_011545295.2:c.806T>C	XP_011543597.1:p.Met269Thr
XM_017018398.2:c.1334T>C	XP_016873887.1:p.Met445Thr
XM_017018399.1:c.794T>C	XP_016873888.1:p.Met265Thr
NM_031471.6:c.1334T>C MANE Select	NP_113659.3:p.Met445Thr
NM_001382361.1:c.1334T>C	NP_001369290.1:p.Met445Thr
NM_001382362.1:c.1346T>C	NP_001369291.1:p.Met449Thr
NM_001382363.1:c.794T>C	NP_001369292.1:p.Met265Thr
NM_001382364.1:c.806T>C	NP_001369293.1:p.Met269Thr
NM_001382448.1:c.1334T>C	NP_001369377.1:p.Met445Thr
NM_178443.3:c.1346T>C	NP_848537.1:p.Met449Thr