Canonical Allele Identifier: CA362299684

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177097550-C-G
• MyVariant Identifiers: chr5:g.176524551C>G (hg19) ; chr5:g.177097550C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097550C>G , CM000667.2:g.177097550C>G	GRCh38
NC_000005.9:g.176524551C>G , CM000667.1:g.176524551C>G	GRCh37
NC_000005.8:g.176457157C>G	NCBI36
NG_012067.1:g.15631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.2283C>G MANE Select	ENSP00000292408.4:p.Phe761Leu
ENST00000292408.8:c.2283C>G	ENSP00000292408.4:p.Phe761Leu
ENST00000393637.5:c.2163C>G	ENSP00000377254.1:p.Phe721Leu
ENST00000393648.6:c.2079C>G	ENSP00000377259.2:p.Phe693Leu
ENST00000502906.5:c.2283C>G	ENSP00000424960.1:p.Phe761Leu
ENST00000513423.1:n.231C>G
NM_001291980.1:c.2079C>G	NP_001278909.1:p.Phe693Leu
NM_002011.4:c.2283C>G	NP_002002.3:p.Phe761Leu
NM_022963.3:c.2163C>G	NP_075252.2:p.Phe721Leu
NM_213647.2:c.2283C>G	NP_998812.1:p.Phe761Leu
XM_005265838.2:c.2283C>G	XP_005265895.1:p.Phe761Leu
XM_011534464.1:c.2376C>G	XP_011532766.1:p.Phe792Leu
XM_011534465.1:c.1965C>G	XP_011532767.1:p.Phe655Leu
NM_001354984.1:c.2283C>G	NP_001341913.1:p.Phe761Leu
NM_213647.3:c.2283C>G MANE Select	NP_998812.1:p.Phe761Leu
NM_001291980.2:c.2079C>G	NP_001278909.1:p.Phe693Leu
NM_001354984.2:c.2283C>G	NP_001341913.1:p.Phe761Leu
NM_002011.5:c.2283C>G	NP_002002.3:p.Phe761Leu