Canonical Allele Identifier: CA447958748

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520152A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093151A>C , CM000667.2:g.177093151A>C	GRCh38
NC_000005.9:g.176520152A>C , CM000667.1:g.176520152A>C	GRCh37
NC_000005.8:g.176452758A>C	NCBI36
NG_012067.1:g.11232A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1071A>C MANE Select	ENSP00000292408.4:p.Thr357=
ENST00000292408.8:c.1071A>C	ENSP00000292408.4:p.Thr357=
ENST00000393637.5:c.1058-181A>C	ENSP00000377254.1:n.1058-181A>C
ENST00000393648.6:c.1071A>C	ENSP00000377259.2:p.Thr357=
ENST00000502906.5:c.1071A>C	ENSP00000424960.1:p.Thr357=
ENST00000508139.1:n.375A>C
NM_001291980.1:c.1071A>C	NP_001278909.1:p.Thr357=
NM_002011.4:c.1071A>C	NP_002002.3:p.Thr357=
NM_022963.3:c.1058-181A>C	NP_075252.2:n.1058-181A>C
NM_213647.2:c.1071A>C	NP_998812.1:p.Thr357=
XM_005265838.2:c.1071A>C	XP_005265895.1:p.Thr357=
XM_011534464.1:c.1164A>C	XP_011532766.1:p.Thr388=
XM_011534465.1:c.753A>C	XP_011532767.1:p.Thr251=
XR_941090.1:n.1116A>C
NM_001354984.1:c.1071A>C	NP_001341913.1:p.Thr357=
NM_213647.3:c.1071A>C MANE Select	NP_998812.1:p.Thr357=
NM_001291980.2:c.1071A>C	NP_001278909.1:p.Thr357=
NM_001354984.2:c.1071A>C	NP_001341913.1:p.Thr357=
NM_002011.5:c.1071A>C	NP_002002.3:p.Thr357=