Canonical Allele Identifier: CA2499307122

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093275_177093276insCCCCC , CM000667.2:g.177093275_177093276insCCCCC	GRCh38
NC_000005.9:g.176520276_176520277insCCCCC , CM000667.1:g.176520276_176520277insCCCCC	GRCh37
NC_000005.8:g.176452882_176452883insCCCCC	NCBI36
NG_012067.1:g.11356_11357insCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1195_1196insCCCCC MANE Select	ENSP00000292408.4:p.His399ProfsTer?
ENST00000292408.8:c.1195_1196insCCCCC	ENSP00000292408.4:p.His399ProfsTer?
ENST00000393637.5:c.1058-57_1058-56insCCCCC	ENSP00000377254.1:n.1058-57_1058-56insCCCCC
ENST00000393648.6:c.1097+98_1097+99insCCCCC	ENSP00000377259.2:n.1097+98_1097+99insCCCCC
ENST00000502906.5:c.1195_1196insCCCCC	ENSP00000424960.1:p.His399ProfsTer?
ENST00000508139.1:n.499_500insCCCCC
ENST00000511076.1:c.101_102insCCCCC
NM_001291980.1:c.1097+98_1097+99insCCCCC	NP_001278909.1:n.1097+98_1097+99insCCCCC
NM_002011.4:c.1195_1196insCCCCC	NP_002002.3:p.His399ProfsTer?
NM_022963.3:c.1058-57_1058-56insCCCCC	NP_075252.2:n.1058-57_1058-56insCCCCC
NM_213647.2:c.1195_1196insCCCCC	NP_998812.1:p.His399ProfsTer?
XM_005265838.2:c.1195_1196insCCCCC	XP_005265895.1:p.His399ProfsTer?
XM_011534464.1:c.1288_1289insCCCCC	XP_011532766.1:p.His430ProfsTer?
XM_011534465.1:c.877_878insCCCCC	XP_011532767.1:p.His293ProfsTer?
XR_941090.1:n.1240_1241insCCCCC
NM_001354984.1:c.1195_1196insCCCCC	NP_001341913.1:p.His399ProfsTer?
NM_213647.3:c.1195_1196insCCCCC MANE Select	NP_998812.1:p.His399ProfsTer?
NM_001291980.2:c.1097+98_1097+99insCCCCC	NP_001278909.1:n.1097+98_1097+99insCCCCC
NM_001354984.2:c.1195_1196insCCCCC	NP_001341913.1:p.His399ProfsTer?
NM_002011.5:c.1195_1196insCCCCC	NP_002002.3:p.His399ProfsTer?