Canonical Allele Identifier: CA447958865

Gene: FGFR4

Linked Data

• dbSNP Id: rs142049814
• MyVariant Identifiers: chr5:g.176520206G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093205G>T , CM000667.2:g.177093205G>T	GRCh38
NC_000005.9:g.176520206G>T , CM000667.1:g.176520206G>T	GRCh37
NC_000005.8:g.176452812G>T	NCBI36
NG_012067.1:g.11286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1125G>T MANE Select	ENSP00000292408.4:p.Ser375=
ENST00000292408.8:c.1125G>T	ENSP00000292408.4:p.Ser375=
ENST00000393637.5:c.1058-127G>T	ENSP00000377254.1:n.1058-127G>T
ENST00000393648.6:c.1097+28G>T	ENSP00000377259.2:n.1097+28G>T
ENST00000502906.5:c.1125G>T	ENSP00000424960.1:p.Ser375=
ENST00000508139.1:n.429G>T
ENST00000511076.1:c.31G>T
NM_001291980.1:c.1097+28G>T	NP_001278909.1:n.1097+28G>T
NM_002011.4:c.1125G>T	NP_002002.3:p.Ser375=
NM_022963.3:c.1058-127G>T	NP_075252.2:n.1058-127G>T
NM_213647.2:c.1125G>T	NP_998812.1:p.Ser375=
XM_005265838.2:c.1125G>T	XP_005265895.1:p.Ser375=
XM_011534464.1:c.1218G>T	XP_011532766.1:p.Ser406=
XM_011534465.1:c.807G>T	XP_011532767.1:p.Ser269=
XR_941090.1:n.1170G>T
NM_001354984.1:c.1125G>T	NP_001341913.1:p.Ser375=
NM_213647.3:c.1125G>T MANE Select	NP_998812.1:p.Ser375=
NM_001291980.2:c.1097+28G>T	NP_001278909.1:n.1097+28G>T
NM_001354984.2:c.1125G>T	NP_001341913.1:p.Ser375=
NM_002011.5:c.1125G>T	NP_002002.3:p.Ser375=