Canonical Allele Identifier: CA2676682120

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093289-C-CCCCCCCCTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093289_177093290insCCCCCCCTTG , CM000667.2:g.177093289_177093290insCCCCCCCTTG	GRCh38
NC_000005.9:g.176520290_176520291insCCCCCCCTTG , CM000667.1:g.176520290_176520291insCCCCCCCTTG	GRCh37
NC_000005.8:g.176452896_176452897insCCCCCCCTTG	NCBI36
NG_012067.1:g.11370_11371insCCCCCCCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1209_1210insCCCCCCCTTG MANE Select	ENSP00000292408.4:p.Ala404ProfsTer?
ENST00000292408.8:c.1209_1210insCCCCCCCTTG	ENSP00000292408.4:p.Ala404ProfsTer?
ENST00000393637.5:c.1058-43_1058-42insCCCCCCCTTG	ENSP00000377254.1:n.1058-43_1058-42insCCCCCCCTTG
ENST00000393648.6:c.1097+112_1097+113insCCCCCCCTTG	ENSP00000377259.2:n.1097+112_1097+113insCCCCCCCTTG
ENST00000502906.5:c.1209_1210insCCCCCCCTTG	ENSP00000424960.1:p.Ala404ProfsTer?
ENST00000508139.1:n.513_514insCCCCCCCTTG
ENST00000511076.1:c.115_116insCCCCCCCTTG
NM_001291980.1:c.1097+112_1097+113insCCCCCCCTTG	NP_001278909.1:n.1097+112_1097+113insCCCCCCCTTG
NM_002011.4:c.1209_1210insCCCCCCCTTG	NP_002002.3:p.Ala404ProfsTer?
NM_022963.3:c.1058-43_1058-42insCCCCCCCTTG	NP_075252.2:n.1058-43_1058-42insCCCCCCCTTG
NM_213647.2:c.1209_1210insCCCCCCCTTG	NP_998812.1:p.Ala404ProfsTer?
XM_005265838.2:c.1209_1210insCCCCCCCTTG	XP_005265895.1:p.Ala404ProfsTer?
XM_011534464.1:c.1302_1303insCCCCCCCTTG	XP_011532766.1:p.Ala435ProfsTer?
XM_011534465.1:c.891_892insCCCCCCCTTG	XP_011532767.1:p.Ala298ProfsTer?
XR_941090.1:n.1254_1255insCCCCCCCTTG
NM_001354984.1:c.1209_1210insCCCCCCCTTG	NP_001341913.1:p.Ala404ProfsTer?
NM_213647.3:c.1209_1210insCCCCCCCTTG MANE Select	NP_998812.1:p.Ala404ProfsTer?
NM_001291980.2:c.1097+112_1097+113insCCCCCCCTTG	NP_001278909.1:n.1097+112_1097+113insCCCCCCCTTG
NM_001354984.2:c.1209_1210insCCCCCCCTTG	NP_001341913.1:p.Ala404ProfsTer?
NM_002011.5:c.1209_1210insCCCCCCCTTG	NP_002002.3:p.Ala404ProfsTer?