Canonical Allele Identifier: CA2711102006

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149735641

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093369G>C , CM000667.2:g.177093369G>C	GRCh38
NC_000005.9:g.176520370G>C , CM000667.1:g.176520370G>C	GRCh37
NC_000005.8:g.176452976G>C	NCBI36
NG_012067.1:g.11450G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1252-37G>C MANE Select	ENSP00000292408.4:n.1252-37G>C
ENST00000292408.8:c.1252-37G>C	ENSP00000292408.4:n.1252-37G>C
ENST00000393637.5:c.1095G>C	ENSP00000377254.1:p.Leu365=
ENST00000393648.6:c.1098-37G>C	ENSP00000377259.2:n.1098-37G>C
ENST00000502906.5:c.1252-37G>C	ENSP00000424960.1:n.1252-37G>C
ENST00000508139.1:n.593G>C
ENST00000511076.1:c.157+38G>C
NM_001291980.1:c.1098-37G>C	NP_001278909.1:n.1098-37G>C
NM_002011.4:c.1252-37G>C	NP_002002.3:n.1252-37G>C
NM_022963.3:c.1095G>C	NP_075252.2:p.Leu365=
NM_213647.2:c.1252-37G>C	NP_998812.1:n.1252-37G>C
XM_005265838.2:c.1252-37G>C	XP_005265895.1:n.1252-37G>C
XM_011534464.1:c.1345-37G>C	XP_011532766.1:n.1345-37G>C
XM_011534465.1:c.934-37G>C	XP_011532767.1:n.934-37G>C
XR_941090.1:n.1297-37G>C
NM_001354984.1:c.1252-37G>C	NP_001341913.1:n.1252-37G>C
NM_213647.3:c.1252-37G>C MANE Select	NP_998812.1:n.1252-37G>C
NM_001291980.2:c.1098-37G>C	NP_001278909.1:n.1098-37G>C
NM_001354984.2:c.1252-37G>C	NP_001341913.1:n.1252-37G>C
NM_002011.5:c.1252-37G>C	NP_002002.3:n.1252-37G>C