Canonical Allele Identifier: CA2676681968

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093112-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093120_177093121del , CM000667.2:g.177093120_177093121del	GRCh38
NC_000005.9:g.176520121_176520122del , CM000667.1:g.176520121_176520122del	GRCh37
NC_000005.8:g.176452727_176452728del	NCBI36
NG_012067.1:g.11201_11202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1058-18_1058-17del MANE Select	ENSP00000292408.4:n.1058-18_1058-17del
ENST00000292408.8:c.1058-18_1058-17del	ENSP00000292408.4:n.1058-18_1058-17del
ENST00000393637.5:c.1058-212_1058-211del	ENSP00000377254.1:n.1058-212_1058-211del
ENST00000393648.6:c.1058-18_1058-17del	ENSP00000377259.2:n.1058-18_1058-17del
ENST00000502906.5:c.1058-18_1058-17del	ENSP00000424960.1:n.1058-18_1058-17del
ENST00000508139.1:n.362-18_362-17del
NM_001291980.1:c.1058-18_1058-17del	NP_001278909.1:n.1058-18_1058-17del
NM_002011.4:c.1058-18_1058-17del	NP_002002.3:n.1058-18_1058-17del
NM_022963.3:c.1058-212_1058-211del	NP_075252.2:n.1058-212_1058-211del
NM_213647.2:c.1058-18_1058-17del	NP_998812.1:n.1058-18_1058-17del
XM_005265838.2:c.1058-18_1058-17del	XP_005265895.1:n.1058-18_1058-17del
XM_011534464.1:c.1151-18_1151-17del	XP_011532766.1:n.1151-18_1151-17del
XM_011534465.1:c.740-18_740-17del	XP_011532767.1:n.740-18_740-17del
XR_941090.1:n.1103-18_1103-17del
NM_001354984.1:c.1058-18_1058-17del	NP_001341913.1:n.1058-18_1058-17del
NM_213647.3:c.1058-18_1058-17del MANE Select	NP_998812.1:n.1058-18_1058-17del
NM_001291980.2:c.1058-18_1058-17del	NP_001278909.1:n.1058-18_1058-17del
NM_001354984.2:c.1058-18_1058-17del	NP_001341913.1:n.1058-18_1058-17del
NM_002011.5:c.1058-18_1058-17del	NP_002002.3:n.1058-18_1058-17del