Canonical Allele Identifier: CA475151807

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64223112-T-C
• MyVariant Identifiers: chr11:g.63990584T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223112T>C , CM000673.2:g.64223112T>C	GRCh38
NC_000011.9:g.63990584T>C , CM000673.1:g.63990584T>C	GRCh37
NC_000011.8:g.63747160T>C	NCBI36
NG_016360.1:g.21433T>C , LRG_180:g.21433T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1747T>C	ENSP00000279227.5:p.Leu583=
ENST00000540554.2:n.3259T>C
ENST00000541252.2:c.1195T>C	ENSP00000438885.2:p.Leu399=
ENST00000544997.6:c.1735T>C	ENSP00000445778.2:p.Leu579=
ENST00000545896.2:c.299T>C	ENSP00000440209.2:p.Leu100Pro
ENST00000546255.2:n.2039T>C
ENST00000698845.1:c.*930T>C	ENSP00000513981.1:n.*930T>C
ENST00000698846.1:n.1981T>C
ENST00000698847.1:c.*1140T>C	ENSP00000513982.1:n.*1140T>C
ENST00000698850.1:n.3756T>C
ENST00000698852.1:c.1735T>C	ENSP00000513984.1:p.Leu579=
ENST00000698853.1:c.*964T>C	ENSP00000513985.1:n.*964T>C
ENST00000698854.1:c.*1065T>C	ENSP00000513986.1:n.*1065T>C
ENST00000698855.1:n.3387T>C
ENST00000698856.1:n.3081T>C
ENST00000698859.1:n.2245T>C
ENST00000698860.1:c.1747T>C	ENSP00000513988.1:p.Leu583=
ENST00000698861.1:c.1735T>C	ENSP00000513989.1:p.Leu579=
ENST00000698862.1:c.*1031T>C	ENSP00000513990.1:n.*1031T>C
ENST00000698863.1:c.1735T>C	ENSP00000513991.1:p.Leu579=
ENST00000698864.1:n.2296T>C
ENST00000698865.1:c.1756T>C	ENSP00000513992.1:p.Leu586=
ENST00000698866.1:c.*1523T>C	ENSP00000513993.1:n.*1523T>C
ENST00000698867.1:n.5710T>C
ENST00000698868.1:c.1600T>C	ENSP00000513994.1:p.Leu534=
ENST00000698869.1:c.1501T>C	ENSP00000513995.1:p.Leu501=
ENST00000698870.1:c.1735T>C	ENSP00000513996.1:p.Leu579=
ENST00000698871.1:n.2258T>C
ENST00000698872.1:c.*524T>C	ENSP00000513997.1:n.*524T>C
ENST00000698873.1:c.*930T>C	ENSP00000513998.1:n.*930T>C
ENST00000698874.1:c.1195T>C	ENSP00000513999.1:p.Leu399=
ENST00000698875.1:n.1595T>C
ENST00000698876.1:n.1783T>C
ENST00000698877.1:n.1303T>C
ENST00000698878.1:c.1729T>C	ENSP00000514000.1:p.Leu577=
ENST00000698880.1:c.1603T>C
ENST00000345728.10:c.1735T>C MANE Select	ENSP00000339950.5:p.Leu579=
ENST00000279227.9:c.1747T>C	ENSP00000279227.5:p.Leu583=
ENST00000345728.9:c.1735T>C	ENSP00000339950.5:p.Leu579=
ENST00000540554.1:n.371T>C
ENST00000545896.1:c.298T>C	ENSP00000440209.1:p.Leu100=
NM_031471.5:c.1735T>C	NP_113659.3:p.Leu579=
NM_178443.2:c.1747T>C , LRG_180t1:c.1747T>C	NP_848537.1:p.Leu583=
XM_011545294.1:c.1747T>C	XP_011543596.1:p.Leu583=
XM_011545295.1:c.1207T>C	XP_011543597.1:p.Leu403=
XM_011545296.1:c.1207T>C	XP_011543598.1:p.Leu403=
XM_011545294.3:c.1747T>C	XP_011543596.1:p.Leu583=
XM_011545295.2:c.1207T>C	XP_011543597.1:p.Leu403=
XM_017018398.2:c.1735T>C	XP_016873887.1:p.Leu579=
XM_017018399.1:c.1195T>C	XP_016873888.1:p.Leu399=
NM_031471.6:c.1735T>C MANE Select	NP_113659.3:p.Leu579=
NM_001382361.1:c.1735T>C	NP_001369290.1:p.Leu579=
NM_001382362.1:c.1747T>C	NP_001369291.1:p.Leu583=
NM_001382363.1:c.1195T>C	NP_001369292.1:p.Leu399=
NM_001382364.1:c.1207T>C	NP_001369293.1:p.Leu403=
NM_001382448.1:c.1735T>C	NP_001369377.1:p.Leu579=
NM_178443.3:c.1747T>C	NP_848537.1:p.Leu583=