Canonical Allele Identifier: CA2676681605

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177092716-A-AATT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092716_177092717insATT , CM000667.2:g.177092716_177092717insATT	GRCh38
NC_000005.9:g.176519717_176519718insATT , CM000667.1:g.176519717_176519718insATT	GRCh37
NC_000005.8:g.176452323_176452324insATT	NCBI36
NG_012067.1:g.10797_10798insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.989_990insATT MANE Select	ENSP00000292408.4:p.Glu330_Tyr331insLeu
ENST00000292408.8:c.989_990insATT	ENSP00000292408.4:p.Glu330_Tyr331insLeu
ENST00000393637.5:c.989_990insATT	ENSP00000377254.1:p.Glu330_Tyr331insLeu
ENST00000393648.6:c.989_990insATT	ENSP00000377259.2:p.Glu330_Tyr331insLeu
ENST00000502906.5:c.989_990insATT	ENSP00000424960.1:p.Glu330_Tyr331insLeu
ENST00000508139.1:n.293_294insATT
ENST00000509511.5:n.989_990insATT
NM_001291980.1:c.989_990insATT	NP_001278909.1:p.Glu330_Tyr331insLeu
NM_002011.4:c.989_990insATT	NP_002002.3:p.Glu330_Tyr331insLeu
NM_022963.3:c.989_990insATT	NP_075252.2:p.Glu330_Tyr331insLeu
NM_213647.2:c.989_990insATT	NP_998812.1:p.Glu330_Tyr331insLeu
XM_005265838.2:c.989_990insATT	XP_005265895.1:p.Glu330_Tyr331insLeu
XM_011534464.1:c.1082_1083insATT	XP_011532766.1:p.Glu361_Tyr362insLeu
XM_011534465.1:c.671_672insATT	XP_011532767.1:p.Glu224_Tyr225insLeu
XR_941090.1:n.1034_1035insATT
NM_001354984.1:c.989_990insATT	NP_001341913.1:p.Glu330_Tyr331insLeu
NM_213647.3:c.989_990insATT MANE Select	NP_998812.1:p.Glu330_Tyr331insLeu
NM_001291980.2:c.989_990insATT	NP_001278909.1:p.Glu330_Tyr331insLeu
NM_001354984.2:c.989_990insATT	NP_001341913.1:p.Glu330_Tyr331insLeu
NM_002011.5:c.989_990insATT	NP_002002.3:p.Glu330_Tyr331insLeu