Canonical Allele Identifier: CA447958808

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520326C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093325C>T , CM000667.2:g.177093325C>T	GRCh38
NC_000005.9:g.176520326C>T , CM000667.1:g.176520326C>T	GRCh37
NC_000005.8:g.176452932C>T	NCBI36
NG_012067.1:g.11406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1245C>T MANE Select	ENSP00000292408.4:p.Ala415=
ENST00000292408.8:c.1245C>T	ENSP00000292408.4:p.Ala415=
ENST00000393637.5:c.1058-7C>T	ENSP00000377254.1:n.1058-7C>T
ENST00000393648.6:c.1098-81C>T	ENSP00000377259.2:n.1098-81C>T
ENST00000502906.5:c.1245C>T	ENSP00000424960.1:p.Ala415=
ENST00000508139.1:n.549C>T
ENST00000511076.1:c.151C>T
NM_001291980.1:c.1098-81C>T	NP_001278909.1:n.1098-81C>T
NM_002011.4:c.1245C>T	NP_002002.3:p.Ala415=
NM_022963.3:c.1058-7C>T	NP_075252.2:n.1058-7C>T
NM_213647.2:c.1245C>T	NP_998812.1:p.Ala415=
XM_005265838.2:c.1245C>T	XP_005265895.1:p.Ala415=
XM_011534464.1:c.1338C>T	XP_011532766.1:p.Ala446=
XM_011534465.1:c.927C>T	XP_011532767.1:p.Ala309=
XR_941090.1:n.1290C>T
NM_001354984.1:c.1245C>T	NP_001341913.1:p.Ala415=
NM_213647.3:c.1245C>T MANE Select	NP_998812.1:p.Ala415=
NM_001291980.2:c.1098-81C>T	NP_001278909.1:n.1098-81C>T
NM_001354984.2:c.1245C>T	NP_001341913.1:p.Ala415=
NM_002011.5:c.1245C>T	NP_002002.3:p.Ala415=