Canonical Allele Identifier: CA362299650

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176524541G>C (hg19) ; chr5:g.177097540G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097540G>C , CM000667.2:g.177097540G>C	GRCh38
NC_000005.9:g.176524541G>C , CM000667.1:g.176524541G>C	GRCh37
NC_000005.8:g.176457147G>C	NCBI36
NG_012067.1:g.15621G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2273G>C MANE Select	ENSP00000292408.4:p.Arg758Pro
ENST00000292408.8:c.2273G>C	ENSP00000292408.4:p.Arg758Pro
ENST00000393637.5:c.2153G>C	ENSP00000377254.1:p.Arg718Pro
ENST00000393648.6:c.2069G>C	ENSP00000377259.2:p.Arg690Pro
ENST00000502906.5:c.2273G>C	ENSP00000424960.1:p.Arg758Pro
ENST00000513423.1:n.221G>C
NM_001291980.1:c.2069G>C	NP_001278909.1:p.Arg690Pro
NM_002011.4:c.2273G>C	NP_002002.3:p.Arg758Pro
NM_022963.3:c.2153G>C	NP_075252.2:p.Arg718Pro
NM_213647.2:c.2273G>C	NP_998812.1:p.Arg758Pro
XM_005265838.2:c.2273G>C	XP_005265895.1:p.Arg758Pro
XM_011534464.1:c.2366G>C	XP_011532766.1:p.Arg789Pro
XM_011534465.1:c.1955G>C	XP_011532767.1:p.Arg652Pro
NM_001354984.1:c.2273G>C	NP_001341913.1:p.Arg758Pro
NM_213647.3:c.2273G>C MANE Select	NP_998812.1:p.Arg758Pro
NM_001291980.2:c.2069G>C	NP_001278909.1:p.Arg690Pro
NM_001354984.2:c.2273G>C	NP_001341913.1:p.Arg758Pro
NM_002011.5:c.2273G>C	NP_002002.3:p.Arg758Pro