Canonical Allele Identifier: CA447959273

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520520T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093519T>C , CM000667.2:g.177093519T>C	GRCh38
NC_000005.9:g.176520520T>C , CM000667.1:g.176520520T>C	GRCh37
NC_000005.8:g.176453126T>C	NCBI36
NG_012067.1:g.11600T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1365T>C MANE Select	ENSP00000292408.4:p.Pro455=
ENST00000292408.8:c.1365T>C	ENSP00000292408.4:p.Pro455=
ENST00000393637.5:c.1245T>C	ENSP00000377254.1:p.Pro415=
ENST00000393648.6:c.1193+18T>C	ENSP00000377259.2:n.1193+18T>C
ENST00000502906.5:c.1365T>C	ENSP00000424960.1:p.Pro455=
ENST00000511076.1:c.259T>C
NM_001291980.1:c.1193+18T>C	NP_001278909.1:n.1193+18T>C
NM_002011.4:c.1365T>C	NP_002002.3:p.Pro455=
NM_022963.3:c.1245T>C	NP_075252.2:p.Pro415=
NM_213647.2:c.1365T>C	NP_998812.1:p.Pro455=
XM_005265838.2:c.1365T>C	XP_005265895.1:p.Pro455=
XM_011534464.1:c.1458T>C	XP_011532766.1:p.Pro486=
XM_011534465.1:c.1047T>C	XP_011532767.1:p.Pro349=
XR_941090.1:n.1392+18T>C
NM_001354984.1:c.1365T>C	NP_001341913.1:p.Pro455=
NM_213647.3:c.1365T>C MANE Select	NP_998812.1:p.Pro455=
NM_001291980.2:c.1193+18T>C	NP_001278909.1:n.1193+18T>C
NM_001354984.2:c.1365T>C	NP_001341913.1:p.Pro455=
NM_002011.5:c.1365T>C	NP_002002.3:p.Pro455=