Canonical Allele Identifier: CA2614108971

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64207306-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64207306C>G , CM000673.2:g.64207306C>G	GRCh38
NC_000011.9:g.63974778C>G , CM000673.1:g.63974778C>G	GRCh37
NC_000011.8:g.63731354C>G	NCBI36
NG_016360.1:g.5627C>G , LRG_180:g.5627C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.-14-45C>G	ENSP00000279227.5:n.-14-45C>G
ENST00000544997.6:c.-11-48C>G	ENSP00000445778.2:n.-11-48C>G
ENST00000546255.2:n.84-48C>G
ENST00000698845.1:c.-11-48C>G	ENSP00000513981.1:n.-11-48C>G
ENST00000698846.1:n.124-45C>G
ENST00000698847.1:c.-14-45C>G	ENSP00000513982.1:n.-14-45C>G
ENST00000698852.1:c.-59C>G	ENSP00000513984.1:n.-59C>G
ENST00000698853.1:c.-14-45C>G	ENSP00000513985.1:n.-14-45C>G
ENST00000698854.1:c.-14-45C>G	ENSP00000513986.1:n.-14-45C>G
ENST00000698859.1:n.151-45C>G
ENST00000698860.1:c.-11-48C>G	ENSP00000513988.1:n.-11-48C>G
ENST00000698861.1:c.-8-51C>G	ENSP00000513989.1:n.-8-51C>G
ENST00000698862.1:c.-14-45C>G	ENSP00000513990.1:n.-14-45C>G
ENST00000698863.1:c.-59C>G	ENSP00000513991.1:n.-59C>G
ENST00000698864.1:n.93-45C>G
ENST00000698865.1:c.-14-45C>G	ENSP00000513992.1:n.-14-45C>G
ENST00000698866.1:c.-14-45C>G	ENSP00000513993.1:n.-14-45C>G
ENST00000698867.1:n.565C>G
ENST00000698868.1:c.-14-45C>G	ENSP00000513994.1:n.-14-45C>G
ENST00000698869.1:c.-14-45C>G	ENSP00000513995.1:n.-14-45C>G
ENST00000698870.1:c.-59C>G	ENSP00000513996.1:n.-59C>G
ENST00000698871.1:n.199C>G
ENST00000698878.1:c.-14-45C>G	ENSP00000514000.1:n.-14-45C>G
ENST00000345728.10:c.-14-45C>G MANE Select	ENSP00000339950.5:n.-14-45C>G
ENST00000279227.9:c.-14-45C>G	ENSP00000279227.5:n.-14-45C>G
ENST00000345728.9:c.-14-45C>G	ENSP00000339950.5:n.-14-45C>G
ENST00000544997.5:c.-11-48C>G	ENSP00000445778.1:n.-11-48C>G
NM_031471.5:c.-14-45C>G	NP_113659.3:n.-14-45C>G
NM_178443.2:c.-14-45C>G , LRG_180t1:c.-14-45C>G	NP_848537.1:n.-14-45C>G
XM_011545294.1:c.-11-48C>G	XP_011543596.1:n.-11-48C>G
XM_011545294.3:c.-11-48C>G	XP_011543596.1:n.-11-48C>G
XM_017018398.2:c.-11-48C>G	XP_016873887.1:n.-11-48C>G
NM_031471.6:c.-14-45C>G MANE Select	NP_113659.3:n.-14-45C>G
NM_001382361.1:c.-11-48C>G	NP_001369290.1:n.-11-48C>G
NM_001382362.1:c.-11-48C>G	NP_001369291.1:n.-11-48C>G
NM_001382448.1:c.-11-48C>G	NP_001369377.1:n.-11-48C>G
NM_178443.3:c.-14-45C>G	NP_848537.1:n.-14-45C>G