Canonical Allele Identifier: CA1978642629

Gene: FERMT3

Linked Data

• dbSNP Id: rs768951292
• gnomAD v4: 11-64223007-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64223007C>T , CM000673.2:g.64223007C>T	GRCh38
NC_000011.9:g.63990479C>T , CM000673.1:g.63990479C>T	GRCh37
NC_000011.8:g.63747055C>T	NCBI36
NG_016360.1:g.21328C>T , LRG_180:g.21328C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000279227.10:c.1683-41C>T	ENSP00000279227.5:n.1683-41C>T
ENST00000540554.2:n.3195-41C>T
ENST00000541252.2:c.1131-41C>T	ENSP00000438885.2:n.1131-41C>T
ENST00000544997.6:c.1671-41C>T	ENSP00000445778.2:n.1671-41C>T
ENST00000545896.2:c.235-41C>T	ENSP00000440209.2:n.235-41C>T
ENST00000546255.2:n.1975-41C>T
ENST00000698845.1:c.*866-41C>T	ENSP00000513981.1:n.*866-41C>T
ENST00000698846.1:n.1917-41C>T
ENST00000698847.1:c.*1076-41C>T	ENSP00000513982.1:n.*1076-41C>T
ENST00000698850.1:n.3651C>T
ENST00000698852.1:c.1671-41C>T	ENSP00000513984.1:n.1671-41C>T
ENST00000698853.1:c.*900-41C>T	ENSP00000513985.1:n.*900-41C>T
ENST00000698854.1:c.*1001-41C>T	ENSP00000513986.1:n.*1001-41C>T
ENST00000698855.1:n.3323-41C>T
ENST00000698856.1:n.3017-41C>T
ENST00000698859.1:n.2181-41C>T
ENST00000698860.1:c.1683-41C>T	ENSP00000513988.1:n.1683-41C>T
ENST00000698861.1:c.1671-41C>T	ENSP00000513989.1:n.1671-41C>T
ENST00000698862.1:c.*967-41C>T	ENSP00000513990.1:n.*967-41C>T
ENST00000698863.1:c.1671-41C>T	ENSP00000513991.1:n.1671-41C>T
ENST00000698864.1:n.2232-41C>T
ENST00000698865.1:c.1692-41C>T	ENSP00000513992.1:n.1692-41C>T
ENST00000698866.1:c.*1459-41C>T	ENSP00000513993.1:n.*1459-41C>T
ENST00000698867.1:n.5646-41C>T
ENST00000698868.1:c.1536-41C>T	ENSP00000513994.1:n.1536-41C>T
ENST00000698869.1:c.1437-41C>T	ENSP00000513995.1:n.1437-41C>T
ENST00000698870.1:c.1671-41C>T	ENSP00000513996.1:n.1671-41C>T
ENST00000698871.1:n.2194-41C>T
ENST00000698872.1:c.*460-41C>T	ENSP00000513997.1:n.*460-41C>T
ENST00000698873.1:c.*866-41C>T	ENSP00000513998.1:n.*866-41C>T
ENST00000698874.1:c.1131-41C>T	ENSP00000513999.1:n.1131-41C>T
ENST00000698875.1:n.1531-41C>T
ENST00000698876.1:n.1719-41C>T
ENST00000698877.1:n.1239-41C>T
ENST00000698878.1:c.1665-41C>T	ENSP00000514000.1:n.1665-41C>T
ENST00000698880.1:c.1539-41C>T
ENST00000345728.10:c.1671-41C>T MANE Select	ENSP00000339950.5:n.1671-41C>T
ENST00000279227.9:c.1683-41C>T	ENSP00000279227.5:n.1683-41C>T
ENST00000345728.9:c.1671-41C>T	ENSP00000339950.5:n.1671-41C>T
ENST00000540554.1:n.307-41C>T
ENST00000545896.1:c.234-41C>T	ENSP00000440209.1:n.234-41C>T
NM_031471.5:c.1671-41C>T	NP_113659.3:n.1671-41C>T
NM_178443.2:c.1683-41C>T , LRG_180t1:c.1683-41C>T	NP_848537.1:n.1683-41C>T
XM_011545294.1:c.1683-41C>T	XP_011543596.1:n.1683-41C>T
XM_011545295.1:c.1143-41C>T	XP_011543597.1:n.1143-41C>T
XM_011545296.1:c.1143-41C>T	XP_011543598.1:n.1143-41C>T
XM_011545294.3:c.1683-41C>T	XP_011543596.1:n.1683-41C>T
XM_011545295.2:c.1143-41C>T	XP_011543597.1:n.1143-41C>T
XM_017018398.2:c.1671-41C>T	XP_016873887.1:n.1671-41C>T
XM_017018399.1:c.1131-41C>T	XP_016873888.1:n.1131-41C>T
NM_031471.6:c.1671-41C>T MANE Select	NP_113659.3:n.1671-41C>T
NM_001382361.1:c.1671-41C>T	NP_001369290.1:n.1671-41C>T
NM_001382362.1:c.1683-41C>T	NP_001369291.1:n.1683-41C>T
NM_001382363.1:c.1131-41C>T	NP_001369292.1:n.1131-41C>T
NM_001382364.1:c.1143-41C>T	NP_001369293.1:n.1143-41C>T
NM_001382448.1:c.1671-41C>T	NP_001369377.1:n.1671-41C>T
NM_178443.3:c.1683-41C>T	NP_848537.1:n.1683-41C>T