Canonical Allele Identifier: CA362293037

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093453-A-G
• MyVariant Identifiers: chr5:g.176520454A>G (hg19) ; chr5:g.177093453A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093453A>G , CM000667.2:g.177093453A>G	GRCh38
NC_000005.9:g.176520454A>G , CM000667.1:g.176520454A>G	GRCh37
NC_000005.8:g.176453060A>G	NCBI36
NG_012067.1:g.11534A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1299A>G MANE Select	ENSP00000292408.4:p.Val433=
ENST00000292408.8:c.1299A>G	ENSP00000292408.4:p.Val433=
ENST00000393637.5:c.1179A>G	ENSP00000377254.1:p.Val393=
ENST00000393648.6:c.1145A>G	ENSP00000377259.2:p.Tyr382Cys
ENST00000502906.5:c.1299A>G	ENSP00000424960.1:p.Val433=
ENST00000508139.1:n.677A>G
ENST00000511076.1:c.193A>G
NM_001291980.1:c.1145A>G	NP_001278909.1:p.Tyr382Cys
NM_002011.4:c.1299A>G	NP_002002.3:p.Val433=
NM_022963.3:c.1179A>G	NP_075252.2:p.Val393=
NM_213647.2:c.1299A>G	NP_998812.1:p.Val433=
XM_005265838.2:c.1299A>G	XP_005265895.1:p.Val433=
XM_011534464.1:c.1392A>G	XP_011532766.1:p.Val464=
XM_011534465.1:c.981A>G	XP_011532767.1:p.Val327=
XR_941090.1:n.1344A>G
NM_001354984.1:c.1299A>G	NP_001341913.1:p.Val433=
NM_213647.3:c.1299A>G MANE Select	NP_998812.1:p.Val433=
NM_001291980.2:c.1145A>G	NP_001278909.1:p.Tyr382Cys
NM_001354984.2:c.1299A>G	NP_001341913.1:p.Val433=
NM_002011.5:c.1299A>G	NP_002002.3:p.Val433=