Canonical Allele Identifier: CA2832609492

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177094455C>A , CM000667.2:g.177094455C>A	GRCh38
NC_000005.9:g.176521456C>A , CM000667.1:g.176521456C>A	GRCh37
NC_000005.8:g.176454062C>A	NCBI36
NG_012067.1:g.12536C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_213647.3:c.1519+680C>A MANE Select	NP_998812.1:n.1519+680C>A
ENST00000292408.9:c.1519+680C>A MANE Select	ENSP00000292408.4:n.1519+680C>A
NM_001291980.1:c.1315+680C>A	NP_001278909.1:n.1315+680C>A
NM_001291980.2:c.1315+680C>A	NP_001278909.1:n.1315+680C>A
NM_001354984.1:c.1519+680C>A	NP_001341913.1:n.1519+680C>A
NM_001354984.2:c.1519+680C>A	NP_001341913.1:n.1519+680C>A
NM_002011.4:c.1519+680C>A	NP_002002.3:n.1519+680C>A
NM_002011.5:c.1519+680C>A	NP_002002.3:n.1519+680C>A
NM_022963.3:c.1399+680C>A	NP_075252.2:n.1399+680C>A
NM_213647.2:c.1519+680C>A	NP_998812.1:n.1519+680C>A
ENST00000292408.8:c.1519+680C>A	ENSP00000292408.4:n.1519+680C>A
ENST00000393637.5:c.1399+680C>A	ENSP00000377254.1:n.1399+680C>A
ENST00000393648.6:c.1315+680C>A	ENSP00000377259.2:n.1315+680C>A
ENST00000502906.5:c.1519+680C>A	ENSP00000424960.1:n.1519+680C>A
ENST00000511076.1:c.413+680C>A
XM_005265838.2:c.1519+680C>A	XP_005265895.1:n.1519+680C>A
XM_011534464.1:c.1612+680C>A	XP_011532766.1:n.1612+680C>A
XM_011534465.1:c.1201+680C>A	XP_011532767.1:n.1201+680C>A
XR_941090.1:n.1514+680C>A