Canonical Allele Identifier: CA679214359

Gene: FERMT3

Linked Data

• dbSNP Id: rs1261273790
• MyVariant Identifiers: chr11:g.63990460del (hg19) ; chr11:g.64222988del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64222988del , CM000673.2:g.64222988del	GRCh38
NC_000011.9:g.63990460del , CM000673.1:g.63990460del	GRCh37
NC_000011.8:g.63747036del	NCBI36
NG_016360.1:g.21309del , LRG_180:g.21309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1683-60del	ENSP00000279227.5:n.1683-60del
ENST00000540554.2:n.3195-60del
ENST00000541252.2:c.1131-60del	ENSP00000438885.2:n.1131-60del
ENST00000544997.6:c.1671-60del	ENSP00000445778.2:n.1671-60del
ENST00000545896.2:c.235-60del	ENSP00000440209.2:n.235-60del
ENST00000546255.2:n.1975-60del
ENST00000698845.1:c.*866-60del	ENSP00000513981.1:n.*866-60del
ENST00000698846.1:n.1917-60del
ENST00000698847.1:c.*1076-60del	ENSP00000513982.1:n.*1076-60del
ENST00000698850.1:n.3632del
ENST00000698852.1:c.1671-60del	ENSP00000513984.1:n.1671-60del
ENST00000698853.1:c.*900-60del	ENSP00000513985.1:n.*900-60del
ENST00000698854.1:c.*1001-60del	ENSP00000513986.1:n.*1001-60del
ENST00000698855.1:n.3323-60del
ENST00000698856.1:n.3017-60del
ENST00000698859.1:n.2181-60del
ENST00000698860.1:c.1683-60del	ENSP00000513988.1:n.1683-60del
ENST00000698861.1:c.1671-60del	ENSP00000513989.1:n.1671-60del
ENST00000698862.1:c.*967-60del	ENSP00000513990.1:n.*967-60del
ENST00000698863.1:c.1671-60del	ENSP00000513991.1:n.1671-60del
ENST00000698864.1:n.2232-60del
ENST00000698865.1:c.1692-60del	ENSP00000513992.1:n.1692-60del
ENST00000698866.1:c.*1459-60del	ENSP00000513993.1:n.*1459-60del
ENST00000698867.1:n.5646-60del
ENST00000698868.1:c.1536-60del	ENSP00000513994.1:n.1536-60del
ENST00000698869.1:c.1437-60del	ENSP00000513995.1:n.1437-60del
ENST00000698870.1:c.1671-60del	ENSP00000513996.1:n.1671-60del
ENST00000698871.1:n.2194-60del
ENST00000698872.1:c.*460-60del	ENSP00000513997.1:n.*460-60del
ENST00000698873.1:c.*866-60del	ENSP00000513998.1:n.*866-60del
ENST00000698874.1:c.1131-60del	ENSP00000513999.1:n.1131-60del
ENST00000698875.1:n.1531-60del
ENST00000698876.1:n.1719-60del
ENST00000698877.1:n.1239-60del
ENST00000698878.1:c.1665-60del	ENSP00000514000.1:n.1665-60del
ENST00000698880.1:c.1539-60del
ENST00000345728.10:c.1671-60del MANE Select	ENSP00000339950.5:n.1671-60del
ENST00000279227.9:c.1683-60del	ENSP00000279227.5:n.1683-60del
ENST00000345728.9:c.1671-60del	ENSP00000339950.5:n.1671-60del
ENST00000540554.1:n.307-60del
ENST00000545896.1:c.234-60del	ENSP00000440209.1:n.234-60del
NM_031471.5:c.1671-60del	NP_113659.3:n.1671-60del
NM_178443.2:c.1683-60del , LRG_180t1:c.1683-60del	NP_848537.1:n.1683-60del
XM_011545294.1:c.1683-60del	XP_011543596.1:n.1683-60del
XM_011545295.1:c.1143-60del	XP_011543597.1:n.1143-60del
XM_011545296.1:c.1143-60del	XP_011543598.1:n.1143-60del
XM_011545294.3:c.1683-60del	XP_011543596.1:n.1683-60del
XM_011545295.2:c.1143-60del	XP_011543597.1:n.1143-60del
XM_017018398.2:c.1671-60del	XP_016873887.1:n.1671-60del
XM_017018399.1:c.1131-60del	XP_016873888.1:n.1131-60del
NM_031471.6:c.1671-60del MANE Select	NP_113659.3:n.1671-60del
NM_001382361.1:c.1671-60del	NP_001369290.1:n.1671-60del
NM_001382362.1:c.1683-60del	NP_001369291.1:n.1683-60del
NM_001382363.1:c.1131-60del	NP_001369292.1:n.1131-60del
NM_001382364.1:c.1143-60del	NP_001369293.1:n.1143-60del
NM_001382448.1:c.1671-60del	NP_001369377.1:n.1671-60del
NM_178443.3:c.1683-60del	NP_848537.1:n.1683-60del