Canonical Allele Identifier: CA362289752

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176519708A>C (hg19) ; chr5:g.177092707A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092707A>C , CM000667.2:g.177092707A>C	GRCh38
NC_000005.9:g.176519708A>C , CM000667.1:g.176519708A>C	GRCh37
NC_000005.8:g.176452314A>C	NCBI36
NG_012067.1:g.10788A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.980A>C MANE Select	ENSP00000292408.4:p.Asp327Ala
ENST00000292408.8:c.980A>C	ENSP00000292408.4:p.Asp327Ala
ENST00000393637.5:c.980A>C	ENSP00000377254.1:p.Asp327Ala
ENST00000393648.6:c.980A>C	ENSP00000377259.2:p.Asp327Ala
ENST00000502906.5:c.980A>C	ENSP00000424960.1:p.Asp327Ala
ENST00000508139.1:n.284A>C
ENST00000509511.5:n.980A>C
NM_001291980.1:c.980A>C	NP_001278909.1:p.Asp327Ala
NM_002011.4:c.980A>C	NP_002002.3:p.Asp327Ala
NM_022963.3:c.980A>C	NP_075252.2:p.Asp327Ala
NM_213647.2:c.980A>C	NP_998812.1:p.Asp327Ala
XM_005265838.2:c.980A>C	XP_005265895.1:p.Asp327Ala
XM_011534464.1:c.1073A>C	XP_011532766.1:p.Asp358Ala
XM_011534465.1:c.662A>C	XP_011532767.1:p.Asp221Ala
XR_941090.1:n.1025A>C
NM_001354984.1:c.980A>C	NP_001341913.1:p.Asp327Ala
NM_213647.3:c.980A>C MANE Select	NP_998812.1:p.Asp327Ala
NM_001291980.2:c.980A>C	NP_001278909.1:p.Asp327Ala
NM_001354984.2:c.980A>C	NP_001341913.1:p.Asp327Ala
NM_002011.5:c.980A>C	NP_002002.3:p.Asp327Ala