Canonical Allele Identifier: CA2676682159
Gene: FGFR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177093298_177093299insGCCAAA , CM000667.2:g.177093298_177093299insGCCAAA GRCh38
NC_000005.9:g.176520299_176520300insGCCAAA , CM000667.1:g.176520299_176520300insGCCAAA GRCh37
NC_000005.8:g.176452905_176452906insGCCAAA NCBI36
NG_012067.1:g.11379_11380insGCCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.1218_1219insGCCAAA MANE Select ENSP00000292408.4:p.Val406_Gln407insAlaLys
ENST00000292408.8:c.1218_1219insGCCAAA ENSP00000292408.4:p.Val406_Gln407insAlaLys
ENST00000393637.5:c.1058-34_1058-33insGCCAAA ENSP00000377254.1:n.1058-34_1058-33insGCCAAA
ENST00000393648.6:c.1098-108_1098-107insGCCAAA ENSP00000377259.2:n.1098-108_1098-107insGCCAAA
ENST00000502906.5:c.1218_1219insGCCAAA ENSP00000424960.1:p.Val406_Gln407insAlaLys
ENST00000508139.1:n.522_523insGCCAAA
ENST00000511076.1:c.124_125insGCCAAA
NM_001291980.1:c.1098-108_1098-107insGCCAAA NP_001278909.1:n.1098-108_1098-107insGCCAAA
NM_002011.4:c.1218_1219insGCCAAA NP_002002.3:p.Val406_Gln407insAlaLys
NM_022963.3:c.1058-34_1058-33insGCCAAA NP_075252.2:n.1058-34_1058-33insGCCAAA
NM_213647.2:c.1218_1219insGCCAAA NP_998812.1:p.Val406_Gln407insAlaLys
XM_005265838.2:c.1218_1219insGCCAAA XP_005265895.1:p.Val406_Gln407insAlaLys
XM_011534464.1:c.1311_1312insGCCAAA XP_011532766.1:p.Val437_Gln438insAlaLys
XM_011534465.1:c.900_901insGCCAAA XP_011532767.1:p.Val300_Gln301insAlaLys
XR_941090.1:n.1263_1264insGCCAAA
NM_001354984.1:c.1218_1219insGCCAAA NP_001341913.1:p.Val406_Gln407insAlaLys
NM_213647.3:c.1218_1219insGCCAAA MANE Select NP_998812.1:p.Val406_Gln407insAlaLys
NM_001291980.2:c.1098-108_1098-107insGCCAAA NP_001278909.1:n.1098-108_1098-107insGCCAAA
NM_001354984.2:c.1218_1219insGCCAAA NP_001341913.1:p.Val406_Gln407insAlaLys
NM_002011.5:c.1218_1219insGCCAAA NP_002002.3:p.Val406_Gln407insAlaLys