Canonical Allele Identifier: CA2676682149

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093294-C-CAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093294_177093295insAGG , CM000667.2:g.177093294_177093295insAGG	GRCh38
NC_000005.9:g.176520295_176520296insAGG , CM000667.1:g.176520295_176520296insAGG	GRCh37
NC_000005.8:g.176452901_176452902insAGG	NCBI36
NG_012067.1:g.11375_11376insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1214_1215insAGG MANE Select	ENSP00000292408.4:p.Thr405_Val406insGly
ENST00000292408.8:c.1214_1215insAGG	ENSP00000292408.4:p.Thr405_Val406insGly
ENST00000393637.5:c.1058-38_1058-37insAGG	ENSP00000377254.1:n.1058-38_1058-37insAGG
ENST00000393648.6:c.1098-112_1098-111insAGG	ENSP00000377259.2:n.1098-112_1098-111insAGG
ENST00000502906.5:c.1214_1215insAGG	ENSP00000424960.1:p.Thr405_Val406insGly
ENST00000508139.1:n.518_519insAGG
ENST00000511076.1:c.120_121insAGG
NM_001291980.1:c.1098-112_1098-111insAGG	NP_001278909.1:n.1098-112_1098-111insAGG
NM_002011.4:c.1214_1215insAGG	NP_002002.3:p.Thr405_Val406insGly
NM_022963.3:c.1058-38_1058-37insAGG	NP_075252.2:n.1058-38_1058-37insAGG
NM_213647.2:c.1214_1215insAGG	NP_998812.1:p.Thr405_Val406insGly
XM_005265838.2:c.1214_1215insAGG	XP_005265895.1:p.Thr405_Val406insGly
XM_011534464.1:c.1307_1308insAGG	XP_011532766.1:p.Thr436_Val437insGly
XM_011534465.1:c.896_897insAGG	XP_011532767.1:p.Thr299_Val300insGly
XR_941090.1:n.1259_1260insAGG
NM_001354984.1:c.1214_1215insAGG	NP_001341913.1:p.Thr405_Val406insGly
NM_213647.3:c.1214_1215insAGG MANE Select	NP_998812.1:p.Thr405_Val406insGly
NM_001291980.2:c.1098-112_1098-111insAGG	NP_001278909.1:n.1098-112_1098-111insAGG
NM_001354984.2:c.1214_1215insAGG	NP_001341913.1:p.Thr405_Val406insGly
NM_002011.5:c.1214_1215insAGG	NP_002002.3:p.Thr405_Val406insGly