Canonical Allele Identifier: CA362299632

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149740912
• MyVariant Identifiers: chr5:g.176524535A>T (hg19) ; chr5:g.177097534A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097534A>T , CM000667.2:g.177097534A>T	GRCh38
NC_000005.9:g.176524535A>T , CM000667.1:g.176524535A>T	GRCh37
NC_000005.8:g.176457141A>T	NCBI36
NG_012067.1:g.15615A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2267A>T MANE Select	ENSP00000292408.4:p.Asp756Val
ENST00000292408.8:c.2267A>T	ENSP00000292408.4:p.Asp756Val
ENST00000393637.5:c.2147A>T	ENSP00000377254.1:p.Asp716Val
ENST00000393648.6:c.2063A>T	ENSP00000377259.2:p.Asp688Val
ENST00000502906.5:c.2267A>T	ENSP00000424960.1:p.Asp756Val
ENST00000513423.1:n.215A>T
NM_001291980.1:c.2063A>T	NP_001278909.1:p.Asp688Val
NM_002011.4:c.2267A>T	NP_002002.3:p.Asp756Val
NM_022963.3:c.2147A>T	NP_075252.2:p.Asp716Val
NM_213647.2:c.2267A>T	NP_998812.1:p.Asp756Val
XM_005265838.2:c.2267A>T	XP_005265895.1:p.Asp756Val
XM_011534464.1:c.2360A>T	XP_011532766.1:p.Asp787Val
XM_011534465.1:c.1949A>T	XP_011532767.1:p.Asp650Val
NM_001354984.1:c.2267A>T	NP_001341913.1:p.Asp756Val
NM_213647.3:c.2267A>T MANE Select	NP_998812.1:p.Asp756Val
NM_001291980.2:c.2063A>T	NP_001278909.1:p.Asp688Val
NM_001354984.2:c.2267A>T	NP_001341913.1:p.Asp756Val
NM_002011.5:c.2267A>T	NP_002002.3:p.Asp756Val