Canonical Allele Identifier: CA362293606

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520537A>G (hg19) ; chr5:g.177093536A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093536A>G , CM000667.2:g.177093536A>G	GRCh38
NC_000005.9:g.176520537A>G , CM000667.1:g.176520537A>G	GRCh37
NC_000005.8:g.176453143A>G	NCBI36
NG_012067.1:g.11617A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1382A>G MANE Select	ENSP00000292408.4:p.Glu461Gly
ENST00000292408.8:c.1382A>G	ENSP00000292408.4:p.Glu461Gly
ENST00000393637.5:c.1262A>G	ENSP00000377254.1:p.Glu421Gly
ENST00000393648.6:c.1193+35A>G	ENSP00000377259.2:n.1193+35A>G
ENST00000502906.5:c.1382A>G	ENSP00000424960.1:p.Glu461Gly
ENST00000511076.1:c.276A>G
NM_001291980.1:c.1193+35A>G	NP_001278909.1:n.1193+35A>G
NM_002011.4:c.1382A>G	NP_002002.3:p.Glu461Gly
NM_022963.3:c.1262A>G	NP_075252.2:p.Glu421Gly
NM_213647.2:c.1382A>G	NP_998812.1:p.Glu461Gly
XM_005265838.2:c.1382A>G	XP_005265895.1:p.Glu461Gly
XM_011534464.1:c.1475A>G	XP_011532766.1:p.Glu492Gly
XM_011534465.1:c.1064A>G	XP_011532767.1:p.Glu355Gly
XR_941090.1:n.1392+35A>G
NM_001354984.1:c.1382A>G	NP_001341913.1:p.Glu461Gly
NM_213647.3:c.1382A>G MANE Select	NP_998812.1:p.Glu461Gly
NM_001291980.2:c.1193+35A>G	NP_001278909.1:n.1193+35A>G
NM_001354984.2:c.1382A>G	NP_001341913.1:p.Glu461Gly
NM_002011.5:c.1382A>G	NP_002002.3:p.Glu461Gly