Canonical Allele Identifier: CA2676681967

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093112-C-CTGTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093116_177093121dup , CM000667.2:g.177093116_177093121dup	GRCh38
NC_000005.9:g.176520117_176520122dup , CM000667.1:g.176520117_176520122dup	GRCh37
NC_000005.8:g.176452723_176452728dup	NCBI36
NG_012067.1:g.11197_11202dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1058-22_1058-17dup MANE Select	ENSP00000292408.4:n.1058-22_1058-17dup
ENST00000292408.8:c.1058-22_1058-17dup	ENSP00000292408.4:n.1058-22_1058-17dup
ENST00000393637.5:c.1058-216_1058-211dup	ENSP00000377254.1:n.1058-216_1058-211dup
ENST00000393648.6:c.1058-22_1058-17dup	ENSP00000377259.2:n.1058-22_1058-17dup
ENST00000502906.5:c.1058-22_1058-17dup	ENSP00000424960.1:n.1058-22_1058-17dup
ENST00000508139.1:n.362-22_362-17dup
NM_001291980.1:c.1058-22_1058-17dup	NP_001278909.1:n.1058-22_1058-17dup
NM_002011.4:c.1058-22_1058-17dup	NP_002002.3:n.1058-22_1058-17dup
NM_022963.3:c.1058-216_1058-211dup	NP_075252.2:n.1058-216_1058-211dup
NM_213647.2:c.1058-22_1058-17dup	NP_998812.1:n.1058-22_1058-17dup
XM_005265838.2:c.1058-22_1058-17dup	XP_005265895.1:n.1058-22_1058-17dup
XM_011534464.1:c.1151-22_1151-17dup	XP_011532766.1:n.1151-22_1151-17dup
XM_011534465.1:c.740-22_740-17dup	XP_011532767.1:n.740-22_740-17dup
XR_941090.1:n.1103-22_1103-17dup
NM_001354984.1:c.1058-22_1058-17dup	NP_001341913.1:n.1058-22_1058-17dup
NM_213647.3:c.1058-22_1058-17dup MANE Select	NP_998812.1:n.1058-22_1058-17dup
NM_001291980.2:c.1058-22_1058-17dup	NP_001278909.1:n.1058-22_1058-17dup
NM_001354984.2:c.1058-22_1058-17dup	NP_001341913.1:n.1058-22_1058-17dup
NM_002011.5:c.1058-22_1058-17dup	NP_002002.3:n.1058-22_1058-17dup