Canonical Allele Identifier: CA362293185

Gene: FGFR4

Linked Data

• dbSNP Id: rs1784442437
• gnomAD v4: 5-177093473-C-T
• MyVariant Identifiers: chr5:g.176520474C>T (hg19) ; chr5:g.177093473C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093473C>T , CM000667.2:g.177093473C>T	GRCh38
NC_000005.9:g.176520474C>T , CM000667.1:g.176520474C>T	GRCh37
NC_000005.8:g.176453080C>T	NCBI36
NG_012067.1:g.11554C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1319C>T MANE Select	ENSP00000292408.4:p.Ser440Phe
ENST00000292408.8:c.1319C>T	ENSP00000292408.4:p.Ser440Phe
ENST00000393637.5:c.1199C>T	ENSP00000377254.1:p.Ser400Phe
ENST00000393648.6:c.1165C>T	ENSP00000377259.2:p.Pro389Ser
ENST00000502906.5:c.1319C>T	ENSP00000424960.1:p.Ser440Phe
ENST00000508139.1:n.697C>T
ENST00000511076.1:c.213C>T
NM_001291980.1:c.1165C>T	NP_001278909.1:p.Pro389Ser
NM_002011.4:c.1319C>T	NP_002002.3:p.Ser440Phe
NM_022963.3:c.1199C>T	NP_075252.2:p.Ser400Phe
NM_213647.2:c.1319C>T	NP_998812.1:p.Ser440Phe
XM_005265838.2:c.1319C>T	XP_005265895.1:p.Ser440Phe
XM_011534464.1:c.1412C>T	XP_011532766.1:p.Ser471Phe
XM_011534465.1:c.1001C>T	XP_011532767.1:p.Ser334Phe
XR_941090.1:n.1364C>T
NM_001354984.1:c.1319C>T	NP_001341913.1:p.Ser440Phe
NM_213647.3:c.1319C>T MANE Select	NP_998812.1:p.Ser440Phe
NM_001291980.2:c.1165C>T	NP_001278909.1:p.Pro389Ser
NM_001354984.2:c.1319C>T	NP_001341913.1:p.Ser440Phe
NM_002011.5:c.1319C>T	NP_002002.3:p.Ser440Phe