Canonical Allele Identifier: CA362290563

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149734990
• MyVariant Identifiers: chr5:g.176520156A>T (hg19) ; chr5:g.177093155A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093155A>T , CM000667.2:g.177093155A>T	GRCh38
NC_000005.9:g.176520156A>T , CM000667.1:g.176520156A>T	GRCh37
NC_000005.8:g.176452762A>T	NCBI36
NG_012067.1:g.11236A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1075A>T MANE Select	ENSP00000292408.4:p.Thr359Ser
ENST00000292408.8:c.1075A>T	ENSP00000292408.4:p.Thr359Ser
ENST00000393637.5:c.1058-177A>T	ENSP00000377254.1:n.1058-177A>T
ENST00000393648.6:c.1075A>T	ENSP00000377259.2:p.Thr359Ser
ENST00000502906.5:c.1075A>T	ENSP00000424960.1:p.Thr359Ser
ENST00000508139.1:n.379A>T
NM_001291980.1:c.1075A>T	NP_001278909.1:p.Thr359Ser
NM_002011.4:c.1075A>T	NP_002002.3:p.Thr359Ser
NM_022963.3:c.1058-177A>T	NP_075252.2:n.1058-177A>T
NM_213647.2:c.1075A>T	NP_998812.1:p.Thr359Ser
XM_005265838.2:c.1075A>T	XP_005265895.1:p.Thr359Ser
XM_011534464.1:c.1168A>T	XP_011532766.1:p.Thr390Ser
XM_011534465.1:c.757A>T	XP_011532767.1:p.Thr253Ser
XR_941090.1:n.1120A>T
NM_001354984.1:c.1075A>T	NP_001341913.1:p.Thr359Ser
NM_213647.3:c.1075A>T MANE Select	NP_998812.1:p.Thr359Ser
NM_001291980.2:c.1075A>T	NP_001278909.1:p.Thr359Ser
NM_001354984.2:c.1075A>T	NP_001341913.1:p.Thr359Ser
NM_002011.5:c.1075A>T	NP_002002.3:p.Thr359Ser