Canonical Allele Identifier: CA3575895

Gene: FGFR4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090325T>C , CM000667.2:g.177090325T>C	GRCh38
NC_000005.9:g.176517326T>C , CM000667.1:g.176517326T>C	GRCh37
NC_000005.8:g.176449932T>C	NCBI36
NG_012067.1:g.8406T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.92-65T>C MANE Select	ENSP00000292408.4:n.92-65T>C
ENST00000292408.8:c.92-65T>C	ENSP00000292408.4:n.92-65T>C
ENST00000393637.5:c.92-65T>C	ENSP00000377254.1:n.92-65T>C
ENST00000393648.6:c.92-65T>C	ENSP00000377259.2:n.92-65T>C
ENST00000426612.5:n.97-65T>C
ENST00000430285.5:c.175-65T>C	ENSP00000395164.1:n.175-65T>C
ENST00000502906.5:c.92-65T>C	ENSP00000424960.1:n.92-65T>C
ENST00000503708.5:c.92-65T>C	ENSP00000424905.1:n.92-65T>C
ENST00000507708.1:n.248-10T>C
ENST00000509511.5:n.92-65T>C
ENST00000510911.5:c.92-65T>C	ENSP00000427222.1:n.92-65T>C
ENST00000513166.1:c.92-65T>C	ENSP00000422889.1:n.92-65T>C
ENST00000514472.1:c.92-65T>C	ENSP00000426492.1:n.92-65T>C
NM_001291980.1:c.92-65T>C	NP_001278909.1:n.92-65T>C
NM_002011.4:c.92-65T>C	NP_002002.3:n.92-65T>C
NM_022963.3:c.92-65T>C	NP_075252.2:n.92-65T>C
NM_213647.2:c.92-65T>C	NP_998812.1:n.92-65T>C
XM_005265838.2:c.92-65T>C	XP_005265895.1:n.92-65T>C
XM_011534464.1:c.185-65T>C	XP_011532766.1:n.185-65T>C
XM_011534465.1:c.-282-10T>C	XP_011532767.1:n.-282-10T>C
XR_941090.1:n.137-65T>C
NM_001354984.1:c.92-65T>C	NP_001341913.1:n.92-65T>C
NM_213647.3:c.92-65T>C MANE Select	NP_998812.1:n.92-65T>C
NM_001291980.2:c.92-65T>C	NP_001278909.1:n.92-65T>C
NM_001354984.2:c.92-65T>C	NP_001341913.1:n.92-65T>C
NM_002011.5:c.92-65T>C	NP_002002.3:n.92-65T>C