Canonical Allele Identifier: CA2676681029

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177091010-T-TTTAATGATA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091010_177091011insTTAATGATA , CM000667.2:g.177091010_177091011insTTAATGATA	GRCh38
NC_000005.9:g.176518011_176518012insTTAATGATA , CM000667.1:g.176518011_176518012insTTAATGATA	GRCh37
NC_000005.8:g.176450617_176450618insTTAATGATA	NCBI36
NG_012067.1:g.9091_9092insTTAATGATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.509_510insTTAATGATA MANE Select	ENSP00000292408.4:p.Phe171Ter
ENST00000292408.8:c.509_510insTTAATGATA	ENSP00000292408.4:p.Phe171Ter
ENST00000393637.5:c.509_510insTTAATGATA	ENSP00000377254.1:p.Phe171Ter
ENST00000393648.6:c.509_510insTTAATGATA	ENSP00000377259.2:p.Phe171Ter
ENST00000426612.5:n.626_627insTTAATGATA
ENST00000430285.5:c.*373_*374insTTAATGATA	ENSP00000395164.1:n.*373_*374insTTAATGATA
ENST00000502906.5:c.509_510insTTAATGATA	ENSP00000424960.1:p.Phe171Ter
ENST00000503708.5:c.509_510insTTAATGATA	ENSP00000424905.1:p.Phe171Ter
ENST00000509511.5:n.509_510insTTAATGATA
NM_001291980.1:c.509_510insTTAATGATA	NP_001278909.1:p.Phe171Ter
NM_002011.4:c.509_510insTTAATGATA	NP_002002.3:p.Phe171Ter
NM_022963.3:c.509_510insTTAATGATA	NP_075252.2:p.Phe171Ter
NM_213647.2:c.509_510insTTAATGATA	NP_998812.1:p.Phe171Ter
XM_005265838.2:c.509_510insTTAATGATA	XP_005265895.1:p.Phe171Ter
XM_011534464.1:c.602_603insTTAATGATA	XP_011532766.1:p.Phe202Ter
XM_011534465.1:c.191_192insTTAATGATA	XP_011532767.1:p.Phe65Ter
XR_941090.1:n.554_555insTTAATGATA
NM_001354984.1:c.509_510insTTAATGATA	NP_001341913.1:p.Phe171Ter
NM_213647.3:c.509_510insTTAATGATA MANE Select	NP_998812.1:p.Phe171Ter
NM_001291980.2:c.509_510insTTAATGATA	NP_001278909.1:p.Phe171Ter
NM_001354984.2:c.509_510insTTAATGATA	NP_001341913.1:p.Phe171Ter
NM_002011.5:c.509_510insTTAATGATA	NP_002002.3:p.Phe171Ter