Canonical Allele Identifier: CA447958779

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520314C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093313C>A , CM000667.2:g.177093313C>A	GRCh38
NC_000005.9:g.176520314C>A , CM000667.1:g.176520314C>A	GRCh37
NC_000005.8:g.176452920C>A	NCBI36
NG_012067.1:g.11394C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1233C>A MANE Select	ENSP00000292408.4:p.Arg411=
ENST00000292408.8:c.1233C>A	ENSP00000292408.4:p.Arg411=
ENST00000393637.5:c.1058-19C>A	ENSP00000377254.1:n.1058-19C>A
ENST00000393648.6:c.1098-93C>A	ENSP00000377259.2:n.1098-93C>A
ENST00000502906.5:c.1233C>A	ENSP00000424960.1:p.Arg411=
ENST00000508139.1:n.537C>A
ENST00000511076.1:c.139C>A
NM_001291980.1:c.1098-93C>A	NP_001278909.1:n.1098-93C>A
NM_002011.4:c.1233C>A	NP_002002.3:p.Arg411=
NM_022963.3:c.1058-19C>A	NP_075252.2:n.1058-19C>A
NM_213647.2:c.1233C>A	NP_998812.1:p.Arg411=
XM_005265838.2:c.1233C>A	XP_005265895.1:p.Arg411=
XM_011534464.1:c.1326C>A	XP_011532766.1:p.Arg442=
XM_011534465.1:c.915C>A	XP_011532767.1:p.Arg305=
XR_941090.1:n.1278C>A
NM_001354984.1:c.1233C>A	NP_001341913.1:p.Arg411=
NM_213647.3:c.1233C>A MANE Select	NP_998812.1:p.Arg411=
NM_001291980.2:c.1098-93C>A	NP_001278909.1:n.1098-93C>A
NM_001354984.2:c.1233C>A	NP_001341913.1:p.Arg411=
NM_002011.5:c.1233C>A	NP_002002.3:p.Arg411=