Canonical Allele Identifier: CA381087759

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63988011T>C (hg19) ; chr11:g.64220539T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220539T>C , CM000673.2:g.64220539T>C	GRCh38
NC_000011.9:g.63988011T>C , CM000673.1:g.63988011T>C	GRCh37
NC_000011.8:g.63744587T>C	NCBI36
NG_016360.1:g.18860T>C , LRG_180:g.18860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1427T>C	ENSP00000279227.5:p.Phe476Ser
ENST00000540554.2:n.2593T>C
ENST00000541252.2:c.875T>C	ENSP00000438885.2:p.Phe292Ser
ENST00000541326.6:n.836T>C
ENST00000544997.6:c.1415T>C	ENSP00000445778.2:p.Phe472Ser
ENST00000545896.2:c.104T>C	ENSP00000440209.2:p.Phe35Ser
ENST00000546255.2:n.1719T>C
ENST00000698845.1:c.*610T>C	ENSP00000513981.1:n.*610T>C
ENST00000698846.1:n.1661T>C
ENST00000698847.1:c.*820T>C	ENSP00000513982.1:n.*820T>C
ENST00000698849.1:n.535T>C
ENST00000698850.1:n.1183T>C
ENST00000698852.1:c.1415T>C	ENSP00000513984.1:p.Phe472Ser
ENST00000698853.1:c.*644T>C	ENSP00000513985.1:n.*644T>C
ENST00000698854.1:c.*745T>C	ENSP00000513986.1:n.*745T>C
ENST00000698855.1:n.3067T>C
ENST00000698856.1:n.2761T>C
ENST00000698859.1:n.1579T>C
ENST00000698860.1:c.1427T>C	ENSP00000513988.1:p.Phe476Ser
ENST00000698861.1:c.1415T>C	ENSP00000513989.1:p.Phe472Ser
ENST00000698862.1:c.*711T>C	ENSP00000513990.1:n.*711T>C
ENST00000698863.1:c.1415T>C	ENSP00000513991.1:p.Phe472Ser
ENST00000698864.1:n.1630T>C
ENST00000698865.1:c.1436T>C	ENSP00000513992.1:p.Phe479Ser
ENST00000698866.1:c.*929T>C	ENSP00000513993.1:n.*929T>C
ENST00000698867.1:n.5390T>C
ENST00000698868.1:c.1280T>C	ENSP00000513994.1:p.Phe427Ser
ENST00000698869.1:c.1311+213T>C	ENSP00000513995.1:n.1311+213T>C
ENST00000698870.1:c.1415T>C	ENSP00000513996.1:p.Phe472Ser
ENST00000698871.1:n.1938T>C
ENST00000698872.1:c.*204T>C	ENSP00000513997.1:n.*204T>C
ENST00000698873.1:c.*610T>C	ENSP00000513998.1:n.*610T>C
ENST00000698874.1:c.875T>C	ENSP00000513999.1:p.Phe292Ser
ENST00000698875.1:n.1275T>C
ENST00000698876.1:n.1463T>C
ENST00000698877.1:n.983T>C
ENST00000698878.1:c.1409T>C	ENSP00000514000.1:p.Phe470Ser
ENST00000698880.1:c.1283T>C
ENST00000345728.10:c.1415T>C MANE Select	ENSP00000339950.5:p.Phe472Ser
ENST00000279227.9:c.1427T>C	ENSP00000279227.5:p.Phe476Ser
ENST00000345728.9:c.1415T>C	ENSP00000339950.5:p.Phe472Ser
ENST00000541326.5:n.831T>C
ENST00000545896.1:c.103T>C	ENSP00000440209.1:p.Ser35Pro
NM_031471.5:c.1415T>C	NP_113659.3:p.Phe472Ser
NM_178443.2:c.1427T>C , LRG_180t1:c.1427T>C	NP_848537.1:p.Phe476Ser
XM_011545294.1:c.1427T>C	XP_011543596.1:p.Phe476Ser
XM_011545295.1:c.887T>C	XP_011543597.1:p.Phe296Ser
XM_011545296.1:c.887T>C	XP_011543598.1:p.Phe296Ser
XM_011545294.3:c.1427T>C	XP_011543596.1:p.Phe476Ser
XM_011545295.2:c.887T>C	XP_011543597.1:p.Phe296Ser
XM_017018398.2:c.1415T>C	XP_016873887.1:p.Phe472Ser
XM_017018399.1:c.875T>C	XP_016873888.1:p.Phe292Ser
NM_031471.6:c.1415T>C MANE Select	NP_113659.3:p.Phe472Ser
NM_001382361.1:c.1415T>C	NP_001369290.1:p.Phe472Ser
NM_001382362.1:c.1427T>C	NP_001369291.1:p.Phe476Ser
NM_001382363.1:c.875T>C	NP_001369292.1:p.Phe292Ser
NM_001382364.1:c.887T>C	NP_001369293.1:p.Phe296Ser
NM_001382448.1:c.1415T>C	NP_001369377.1:p.Phe472Ser
NM_178443.3:c.1427T>C	NP_848537.1:p.Phe476Ser