Canonical Allele Identifier: CA362299657

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176524543C>A (hg19) ; chr5:g.177097542C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097542C>A , CM000667.2:g.177097542C>A	GRCh38
NC_000005.9:g.176524543C>A , CM000667.1:g.176524543C>A	GRCh37
NC_000005.8:g.176457149C>A	NCBI36
NG_012067.1:g.15623C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2275C>A MANE Select	ENSP00000292408.4:p.Leu759Met
ENST00000292408.8:c.2275C>A	ENSP00000292408.4:p.Leu759Met
ENST00000393637.5:c.2155C>A	ENSP00000377254.1:p.Leu719Met
ENST00000393648.6:c.2071C>A	ENSP00000377259.2:p.Leu691Met
ENST00000502906.5:c.2275C>A	ENSP00000424960.1:p.Leu759Met
ENST00000513423.1:n.223C>A
NM_001291980.1:c.2071C>A	NP_001278909.1:p.Leu691Met
NM_002011.4:c.2275C>A	NP_002002.3:p.Leu759Met
NM_022963.3:c.2155C>A	NP_075252.2:p.Leu719Met
NM_213647.2:c.2275C>A	NP_998812.1:p.Leu759Met
XM_005265838.2:c.2275C>A	XP_005265895.1:p.Leu759Met
XM_011534464.1:c.2368C>A	XP_011532766.1:p.Leu790Met
XM_011534465.1:c.1957C>A	XP_011532767.1:p.Leu653Met
NM_001354984.1:c.2275C>A	NP_001341913.1:p.Leu759Met
NM_213647.3:c.2275C>A MANE Select	NP_998812.1:p.Leu759Met
NM_001291980.2:c.2071C>A	NP_001278909.1:p.Leu691Met
NM_001354984.2:c.2275C>A	NP_001341913.1:p.Leu759Met
NM_002011.5:c.2275C>A	NP_002002.3:p.Leu759Met