Canonical Allele Identifier: CA1603397436

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093532_177093533delinsTG , CM000667.2:g.177093532_177093533delinsTG	GRCh38
NC_000005.9:g.176520533_176520534delinsTG , CM000667.1:g.176520533_176520534delinsTG	GRCh37
NC_000005.8:g.176453139_176453140delinsTG	NCBI36
NG_012067.1:g.11613_11614delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1378_1379delinsTG MANE Select	ENSP00000292408.4:p.Trp460=
ENST00000292408.8:c.1378_1379delinsTG	ENSP00000292408.4:p.Trp460=
ENST00000393637.5:c.1258_1259delinsTG	ENSP00000377254.1:p.Trp420=
ENST00000393648.6:c.1193+31_1193+32delinsTG	ENSP00000377259.2:n.1193+31_1193+32delinsTG
ENST00000502906.5:c.1378_1379delinsTG	ENSP00000424960.1:p.Trp460=
ENST00000511076.1:c.272_273delinsTG
NM_001291980.1:c.1193+31_1193+32delinsTG	NP_001278909.1:n.1193+31_1193+32delinsTG
NM_002011.4:c.1378_1379delinsTG	NP_002002.3:p.Trp460=
NM_022963.3:c.1258_1259delinsTG	NP_075252.2:p.Trp420=
NM_213647.2:c.1378_1379delinsTG	NP_998812.1:p.Trp460=
XM_005265838.2:c.1378_1379delinsTG	XP_005265895.1:p.Trp460=
XM_011534464.1:c.1471_1472delinsTG	XP_011532766.1:p.Trp491=
XM_011534465.1:c.1060_1061delinsTG	XP_011532767.1:p.Trp354=
XR_941090.1:n.1392+31_1392+32delinsTG
NM_001354984.1:c.1378_1379delinsTG	NP_001341913.1:p.Trp460=
NM_213647.3:c.1378_1379delinsTG MANE Select	NP_998812.1:p.Trp460=
NM_001291980.2:c.1193+31_1193+32delinsTG	NP_001278909.1:n.1193+31_1193+32delinsTG
NM_001354984.2:c.1378_1379delinsTG	NP_001341913.1:p.Trp460=
NM_002011.5:c.1378_1379delinsTG	NP_002002.3:p.Trp460=