Canonical Allele Identifier: CA362293718

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093548-A-T
• MyVariant Identifiers: chr5:g.176520549A>T (hg19) ; chr5:g.177093548A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093548A>T , CM000667.2:g.177093548A>T	GRCh38
NC_000005.9:g.176520549A>T , CM000667.1:g.176520549A>T	GRCh37
NC_000005.8:g.176453155A>T	NCBI36
NG_012067.1:g.11629A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1394A>T MANE Select	ENSP00000292408.4:p.Asp465Val
ENST00000292408.8:c.1394A>T	ENSP00000292408.4:p.Asp465Val
ENST00000393637.5:c.1274A>T	ENSP00000377254.1:p.Asp425Val
ENST00000393648.6:c.1193+47A>T	ENSP00000377259.2:n.1193+47A>T
ENST00000502906.5:c.1394A>T	ENSP00000424960.1:p.Asp465Val
ENST00000511076.1:c.288A>T
NM_001291980.1:c.1193+47A>T	NP_001278909.1:n.1193+47A>T
NM_002011.4:c.1394A>T	NP_002002.3:p.Asp465Val
NM_022963.3:c.1274A>T	NP_075252.2:p.Asp425Val
NM_213647.2:c.1394A>T	NP_998812.1:p.Asp465Val
XM_005265838.2:c.1394A>T	XP_005265895.1:p.Asp465Val
XM_011534464.1:c.1487A>T	XP_011532766.1:p.Asp496Val
XM_011534465.1:c.1076A>T	XP_011532767.1:p.Asp359Val
XR_941090.1:n.1392+47A>T
NM_001354984.1:c.1394A>T	NP_001341913.1:p.Asp465Val
NM_213647.3:c.1394A>T MANE Select	NP_998812.1:p.Asp465Val
NM_001291980.2:c.1193+47A>T	NP_001278909.1:n.1193+47A>T
NM_001354984.2:c.1394A>T	NP_001341913.1:p.Asp465Val
NM_002011.5:c.1394A>T	NP_002002.3:p.Asp465Val