Canonical Allele Identifier: CA362286739

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176517817C>A (hg19) ; chr5:g.177090816C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090816C>A , CM000667.2:g.177090816C>A	GRCh38
NC_000005.9:g.176517817C>A , CM000667.1:g.176517817C>A	GRCh37
NC_000005.8:g.176450423C>A	NCBI36
NG_012067.1:g.8897C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.427C>A MANE Select	ENSP00000292408.4:p.Pro143Thr
ENST00000292408.8:c.427C>A	ENSP00000292408.4:p.Pro143Thr
ENST00000393637.5:c.427C>A	ENSP00000377254.1:p.Pro143Thr
ENST00000393648.6:c.427C>A	ENSP00000377259.2:p.Pro143Thr
ENST00000426612.5:n.432C>A
ENST00000430285.5:c.*291C>A	ENSP00000395164.1:n.*291C>A
ENST00000502906.5:c.427C>A	ENSP00000424960.1:p.Pro143Thr
ENST00000503708.5:c.427C>A	ENSP00000424905.1:p.Pro143Thr
ENST00000509511.5:n.427C>A
NM_001291980.1:c.427C>A	NP_001278909.1:p.Pro143Thr
NM_002011.4:c.427C>A	NP_002002.3:p.Pro143Thr
NM_022963.3:c.427C>A	NP_075252.2:p.Pro143Thr
NM_213647.2:c.427C>A	NP_998812.1:p.Pro143Thr
XM_005265838.2:c.427C>A	XP_005265895.1:p.Pro143Thr
XM_011534464.1:c.520C>A	XP_011532766.1:p.Pro174Thr
XM_011534465.1:c.109C>A	XP_011532767.1:p.Pro37Thr
XR_941090.1:n.472C>A
NM_001354984.1:c.427C>A	NP_001341913.1:p.Pro143Thr
NM_213647.3:c.427C>A MANE Select	NP_998812.1:p.Pro143Thr
NM_001291980.2:c.427C>A	NP_001278909.1:p.Pro143Thr
NM_001354984.2:c.427C>A	NP_001341913.1:p.Pro143Thr
NM_002011.5:c.427C>A	NP_002002.3:p.Pro143Thr