Canonical Allele Identifier: CA2676682275

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093476-GCGGCCCCGCCTTGCTCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093482_177093499del , CM000667.2:g.177093482_177093499del	GRCh38
NC_000005.9:g.176520483_176520500del , CM000667.1:g.176520483_176520500del	GRCh37
NC_000005.8:g.176453089_176453106del	NCBI36
NG_012067.1:g.11563_11580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1328_1345del MANE Select	ENSP00000292408.4:p.Pro443_Gly448del
ENST00000292408.8:c.1328_1345del	ENSP00000292408.4:p.Pro443_Gly448del
ENST00000393637.5:c.1208_1225del	ENSP00000377254.1:p.Pro403_Gly408del
ENST00000393648.6:c.1174_1191del	ENSP00000377259.2:p.Pro392_Ala397del
ENST00000502906.5:c.1328_1345del	ENSP00000424960.1:p.Pro443_Gly448del
ENST00000511076.1:c.222_239del
NM_001291980.1:c.1174_1191del	NP_001278909.1:p.Pro392_Ala397del
NM_002011.4:c.1328_1345del	NP_002002.3:p.Pro443_Gly448del
NM_022963.3:c.1208_1225del	NP_075252.2:p.Pro403_Gly408del
NM_213647.2:c.1328_1345del	NP_998812.1:p.Pro443_Gly448del
XM_005265838.2:c.1328_1345del	XP_005265895.1:p.Pro443_Gly448del
XM_011534464.1:c.1421_1438del	XP_011532766.1:p.Pro474_Gly479del
XM_011534465.1:c.1010_1027del	XP_011532767.1:p.Pro337_Gly342del
XR_941090.1:n.1373_1390del
NM_001354984.1:c.1328_1345del	NP_001341913.1:p.Pro443_Gly448del
NM_213647.3:c.1328_1345del MANE Select	NP_998812.1:p.Pro443_Gly448del
NM_001291980.2:c.1174_1191del	NP_001278909.1:p.Pro392_Ala397del
NM_001354984.2:c.1328_1345del	NP_001341913.1:p.Pro443_Gly448del
NM_002011.5:c.1328_1345del	NP_002002.3:p.Pro443_Gly448del