Canonical Allele Identifier: CA1429673065

Gene: FGF12

Linked Data

• dbSNP Id: rs1718876066

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192364350_192364351del , CM000665.2:g.192364350_192364351del	GRCh38
NC_000003.11:g.192082139_192082140del , CM000665.1:g.192082139_192082140del	GRCh37
NC_000003.10:g.193564833_193564834del	NCBI36
NG_051966.1:g.368252_368253del

Transcript Alleles

HGVS	Amino-acid change
ENST00000454309.7:c.200-3810_200-3809del	ENSP00000413496.2:n.200-3810_200-3809del
ENST00000682819.2:n.267-3810_267-3809del
ENST00000683451.2:c.14-3810_14-3809del	ENSP00000508366.1:n.14-3810_14-3809del
ENST00000682572.1:n.202-3810_202-3809del
ENST00000682819.1:n.233-3810_233-3809del
ENST00000683451.1:c.14-3810_14-3809del	ENSP00000508366.1:n.14-3810_14-3809del
ENST00000683935.1:c.14-3810_14-3809del	ENSP00000507098.1:n.14-3810_14-3809del
ENST00000684282.1:c.-59-3810_-59-3809del	ENSP00000507149.1:n.-59-3810_-59-3809del
ENST00000684728.1:c.-59-3810_-59-3809del	ENSP00000506839.1:n.-59-3810_-59-3809del
ENST00000445105.7:c.14-3810_14-3809del MANE Select	ENSP00000393686.1:n.14-3810_14-3809del
ENST00000418610.1:c.14-3810_14-3809del	ENSP00000395517.1:n.14-3810_14-3809del
ENST00000430714.5:c.14-28884_14-28883del	ENSP00000410125.1:n.14-28884_14-28883del
ENST00000445105.6:c.14-3810_14-3809del	ENSP00000393686.1:n.14-3810_14-3809del
ENST00000448795.5:c.-59-3810_-59-3809del	ENSP00000412904.1:n.-59-3810_-59-3809del
ENST00000450716.5:c.14-3810_14-3809del	ENSP00000397635.1:n.14-3810_14-3809del
ENST00000454309.6:c.200-3810_200-3809del	ENSP00000413496.2:n.200-3810_200-3809del
NM_004113.5:c.14-3810_14-3809del	NP_004104.3:n.14-3810_14-3809del
NM_021032.4:c.200-3810_200-3809del	NP_066360.1:n.200-3810_200-3809del
XM_005247227.1:c.92-3810_92-3809del	XP_005247284.1:n.92-3810_92-3809del
XM_006713538.2:c.5-3810_5-3809del	XP_006713601.1:n.5-3810_5-3809del
XM_005247227.2:c.92-3810_92-3809del	XP_005247284.1:n.92-3810_92-3809del
XM_006713538.3:c.5-3810_5-3809del	XP_006713601.1:n.5-3810_5-3809del
NM_001377292.1:c.14-28884_14-28883del	NP_001364221.1:n.14-28884_14-28883del
NM_001377293.1:c.-59-3810_-59-3809del	NP_001364222.1:n.-59-3810_-59-3809del
NM_001377294.1:c.-59-3810_-59-3809del	NP_001364223.1:n.-59-3810_-59-3809del
NM_004113.6:c.14-3810_14-3809del MANE Select	NP_004104.3:n.14-3810_14-3809del
NM_021032.5:c.200-3810_200-3809del	NP_066360.1:n.200-3810_200-3809del