Canonical Allele Identifier: CA2676682160

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093298-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093299_177093300del , CM000667.2:g.177093299_177093300del	GRCh38
NC_000005.9:g.176520300_176520301del , CM000667.1:g.176520300_176520301del	GRCh37
NC_000005.8:g.176452906_176452907del	NCBI36
NG_012067.1:g.11380_11381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1219_1220del MANE Select	ENSP00000292408.4:p.Gln407GlufsTer?
ENST00000292408.8:c.1219_1220del	ENSP00000292408.4:p.Gln407GlufsTer?
ENST00000393637.5:c.1058-33_1058-32del	ENSP00000377254.1:n.1058-33_1058-32del
ENST00000393648.6:c.1098-107_1098-106del	ENSP00000377259.2:n.1098-107_1098-106del
ENST00000502906.5:c.1219_1220del	ENSP00000424960.1:p.Gln407GlufsTer?
ENST00000508139.1:n.523_524del
ENST00000511076.1:c.125_126del
NM_001291980.1:c.1098-107_1098-106del	NP_001278909.1:n.1098-107_1098-106del
NM_002011.4:c.1219_1220del	NP_002002.3:p.Gln407GlufsTer?
NM_022963.3:c.1058-33_1058-32del	NP_075252.2:n.1058-33_1058-32del
NM_213647.2:c.1219_1220del	NP_998812.1:p.Gln407GlufsTer?
XM_005265838.2:c.1219_1220del	XP_005265895.1:p.Gln407GlufsTer?
XM_011534464.1:c.1312_1313del	XP_011532766.1:p.Gln438GlufsTer?
XM_011534465.1:c.901_902del	XP_011532767.1:p.Gln301GlufsTer?
XR_941090.1:n.1264_1265del
NM_001354984.1:c.1219_1220del	NP_001341913.1:p.Gln407GlufsTer?
NM_213647.3:c.1219_1220del MANE Select	NP_998812.1:p.Gln407GlufsTer?
NM_001291980.2:c.1098-107_1098-106del	NP_001278909.1:n.1098-107_1098-106del
NM_001354984.2:c.1219_1220del	NP_001341913.1:p.Gln407GlufsTer?
NM_002011.5:c.1219_1220del	NP_002002.3:p.Gln407GlufsTer?