Canonical Allele Identifier: CA2739871155

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092956G>C , CM000667.2:g.177092956G>C	GRCh38
NC_000005.9:g.176519957G>C , CM000667.1:g.176519957G>C	GRCh37
NC_000005.8:g.176452563G>C	NCBI36
NG_012067.1:g.11037G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1057+172G>C MANE Select	ENSP00000292408.4:n.1057+172G>C
ENST00000292408.8:c.1057+172G>C	ENSP00000292408.4:n.1057+172G>C
ENST00000393637.5:c.1057+172G>C	ENSP00000377254.1:n.1057+172G>C
ENST00000393648.6:c.1057+172G>C	ENSP00000377259.2:n.1057+172G>C
ENST00000502906.5:c.1057+172G>C	ENSP00000424960.1:n.1057+172G>C
ENST00000508139.1:n.361+172G>C
ENST00000509511.5:n.1229G>C
NM_001291980.1:c.1057+172G>C	NP_001278909.1:n.1057+172G>C
NM_002011.4:c.1057+172G>C	NP_002002.3:n.1057+172G>C
NM_022963.3:c.1057+172G>C	NP_075252.2:n.1057+172G>C
NM_213647.2:c.1057+172G>C	NP_998812.1:n.1057+172G>C
XM_005265838.2:c.1057+172G>C	XP_005265895.1:n.1057+172G>C
XM_011534464.1:c.1150+172G>C	XP_011532766.1:n.1150+172G>C
XM_011534465.1:c.739+172G>C	XP_011532767.1:n.739+172G>C
XR_941090.1:n.1102+172G>C
NM_001354984.1:c.1057+172G>C	NP_001341913.1:n.1057+172G>C
NM_213647.3:c.1057+172G>C MANE Select	NP_998812.1:n.1057+172G>C
NM_001291980.2:c.1057+172G>C	NP_001278909.1:n.1057+172G>C
NM_001354984.2:c.1057+172G>C	NP_001341913.1:n.1057+172G>C
NM_002011.5:c.1057+172G>C	NP_002002.3:n.1057+172G>C