Canonical Allele Identifier: CA2676682152

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093294-C-CCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093294_177093295insCCT , CM000667.2:g.177093294_177093295insCCT	GRCh38
NC_000005.9:g.176520295_176520296insCCT , CM000667.1:g.176520295_176520296insCCT	GRCh37
NC_000005.8:g.176452901_176452902insCCT	NCBI36
NG_012067.1:g.11375_11376insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1214_1215insCCT MANE Select	ENSP00000292408.4:p.Thr405_Val406insLeu
ENST00000292408.8:c.1214_1215insCCT	ENSP00000292408.4:p.Thr405_Val406insLeu
ENST00000393637.5:c.1058-38_1058-37insCCT	ENSP00000377254.1:n.1058-38_1058-37insCCT
ENST00000393648.6:c.1098-112_1098-111insCCT	ENSP00000377259.2:n.1098-112_1098-111insCCT
ENST00000502906.5:c.1214_1215insCCT	ENSP00000424960.1:p.Thr405_Val406insLeu
ENST00000508139.1:n.518_519insCCT
ENST00000511076.1:c.120_121insCCT
NM_001291980.1:c.1098-112_1098-111insCCT	NP_001278909.1:n.1098-112_1098-111insCCT
NM_002011.4:c.1214_1215insCCT	NP_002002.3:p.Thr405_Val406insLeu
NM_022963.3:c.1058-38_1058-37insCCT	NP_075252.2:n.1058-38_1058-37insCCT
NM_213647.2:c.1214_1215insCCT	NP_998812.1:p.Thr405_Val406insLeu
XM_005265838.2:c.1214_1215insCCT	XP_005265895.1:p.Thr405_Val406insLeu
XM_011534464.1:c.1307_1308insCCT	XP_011532766.1:p.Thr436_Val437insLeu
XM_011534465.1:c.896_897insCCT	XP_011532767.1:p.Thr299_Val300insLeu
XR_941090.1:n.1259_1260insCCT
NM_001354984.1:c.1214_1215insCCT	NP_001341913.1:p.Thr405_Val406insLeu
NM_213647.3:c.1214_1215insCCT MANE Select	NP_998812.1:p.Thr405_Val406insLeu
NM_001291980.2:c.1098-112_1098-111insCCT	NP_001278909.1:n.1098-112_1098-111insCCT
NM_001354984.2:c.1214_1215insCCT	NP_001341913.1:p.Thr405_Val406insLeu
NM_002011.5:c.1214_1215insCCT	NP_002002.3:p.Thr405_Val406insLeu