Canonical Allele Identifier: CA1603396853

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093183_177093184delinsCG , CM000667.2:g.177093183_177093184delinsCG	GRCh38
NC_000005.9:g.176520184_176520185delinsCG , CM000667.1:g.176520184_176520185delinsCG	GRCh37
NC_000005.8:g.176452790_176452791delinsCG	NCBI36
NG_012067.1:g.11264_11265delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1103_1104delinsCG MANE Select	ENSP00000292408.4:p.Thr368=
ENST00000292408.8:c.1103_1104delinsCG	ENSP00000292408.4:p.Thr368=
ENST00000393637.5:c.1058-149_1058-148delinsCG	ENSP00000377254.1:n.1058-149_1058-148delinsCG
ENST00000393648.6:c.1097+6_1097+7delinsCG	ENSP00000377259.2:n.1097+6_1097+7delinsCG
ENST00000502906.5:c.1103_1104delinsCG	ENSP00000424960.1:p.Thr368=
ENST00000508139.1:n.407_408delinsCG
ENST00000511076.1:c.9_10delinsCG
NM_001291980.1:c.1097+6_1097+7delinsCG	NP_001278909.1:n.1097+6_1097+7delinsCG
NM_002011.4:c.1103_1104delinsCG	NP_002002.3:p.Thr368=
NM_022963.3:c.1058-149_1058-148delinsCG	NP_075252.2:n.1058-149_1058-148delinsCG
NM_213647.2:c.1103_1104delinsCG	NP_998812.1:p.Thr368=
XM_005265838.2:c.1103_1104delinsCG	XP_005265895.1:p.Thr368=
XM_011534464.1:c.1196_1197delinsCG	XP_011532766.1:p.Thr399=
XM_011534465.1:c.785_786delinsCG	XP_011532767.1:p.Thr262=
XR_941090.1:n.1148_1149delinsCG
NM_001354984.1:c.1103_1104delinsCG	NP_001341913.1:p.Thr368=
NM_213647.3:c.1103_1104delinsCG MANE Select	NP_998812.1:p.Thr368=
NM_001291980.2:c.1097+6_1097+7delinsCG	NP_001278909.1:n.1097+6_1097+7delinsCG
NM_001354984.2:c.1103_1104delinsCG	NP_001341913.1:p.Thr368=
NM_002011.5:c.1103_1104delinsCG	NP_002002.3:p.Thr368=