Canonical Allele Identifier: CA362299639

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176524537C>G (hg19) ; chr5:g.177097536C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097536C>G , CM000667.2:g.177097536C>G	GRCh38
NC_000005.9:g.176524537C>G , CM000667.1:g.176524537C>G	GRCh37
NC_000005.8:g.176457143C>G	NCBI36
NG_012067.1:g.15617C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2269C>G MANE Select	ENSP00000292408.4:p.Leu757Val
ENST00000292408.8:c.2269C>G	ENSP00000292408.4:p.Leu757Val
ENST00000393637.5:c.2149C>G	ENSP00000377254.1:p.Leu717Val
ENST00000393648.6:c.2065C>G	ENSP00000377259.2:p.Leu689Val
ENST00000502906.5:c.2269C>G	ENSP00000424960.1:p.Leu757Val
ENST00000513423.1:n.217C>G
NM_001291980.1:c.2065C>G	NP_001278909.1:p.Leu689Val
NM_002011.4:c.2269C>G	NP_002002.3:p.Leu757Val
NM_022963.3:c.2149C>G	NP_075252.2:p.Leu717Val
NM_213647.2:c.2269C>G	NP_998812.1:p.Leu757Val
XM_005265838.2:c.2269C>G	XP_005265895.1:p.Leu757Val
XM_011534464.1:c.2362C>G	XP_011532766.1:p.Leu788Val
XM_011534465.1:c.1951C>G	XP_011532767.1:p.Leu651Val
NM_001354984.1:c.2269C>G	NP_001341913.1:p.Leu757Val
NM_213647.3:c.2269C>G MANE Select	NP_998812.1:p.Leu757Val
NM_001291980.2:c.2065C>G	NP_001278909.1:p.Leu689Val
NM_001354984.2:c.2269C>G	NP_001341913.1:p.Leu757Val
NM_002011.5:c.2269C>G	NP_002002.3:p.Leu757Val