Canonical Allele Identifier: CA2676681858

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093051-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093051_177093052insC , CM000667.2:g.177093051_177093052insC	GRCh38
NC_000005.9:g.176520052_176520053insC , CM000667.1:g.176520052_176520053insC	GRCh37
NC_000005.8:g.176452658_176452659insC	NCBI36
NG_012067.1:g.11132_11133insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1058-87_1058-86insC MANE Select	ENSP00000292408.4:n.1058-87_1058-86insC
ENST00000292408.8:c.1058-87_1058-86insC	ENSP00000292408.4:n.1058-87_1058-86insC
ENST00000393637.5:c.1057+267_1057+268insC	ENSP00000377254.1:n.1057+267_1057+268insC
ENST00000393648.6:c.1058-87_1058-86insC	ENSP00000377259.2:n.1058-87_1058-86insC
ENST00000502906.5:c.1058-87_1058-86insC	ENSP00000424960.1:n.1058-87_1058-86insC
ENST00000508139.1:n.362-87_362-86insC
ENST00000509511.5:n.1324_1325insC
NM_001291980.1:c.1058-87_1058-86insC	NP_001278909.1:n.1058-87_1058-86insC
NM_002011.4:c.1058-87_1058-86insC	NP_002002.3:n.1058-87_1058-86insC
NM_022963.3:c.1057+267_1057+268insC	NP_075252.2:n.1057+267_1057+268insC
NM_213647.2:c.1058-87_1058-86insC	NP_998812.1:n.1058-87_1058-86insC
XM_005265838.2:c.1058-87_1058-86insC	XP_005265895.1:n.1058-87_1058-86insC
XM_011534464.1:c.1151-87_1151-86insC	XP_011532766.1:n.1151-87_1151-86insC
XM_011534465.1:c.740-87_740-86insC	XP_011532767.1:n.740-87_740-86insC
XR_941090.1:n.1103-87_1103-86insC
NM_001354984.1:c.1058-87_1058-86insC	NP_001341913.1:n.1058-87_1058-86insC
NM_213647.3:c.1058-87_1058-86insC MANE Select	NP_998812.1:n.1058-87_1058-86insC
NM_001291980.2:c.1058-87_1058-86insC	NP_001278909.1:n.1058-87_1058-86insC
NM_001354984.2:c.1058-87_1058-86insC	NP_001341913.1:n.1058-87_1058-86insC
NM_002011.5:c.1058-87_1058-86insC	NP_002002.3:n.1058-87_1058-86insC