Canonical Allele Identifier: CA362287112

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176518077A>C (hg19) ; chr5:g.177091076A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091076A>C , CM000667.2:g.177091076A>C	GRCh38
NC_000005.9:g.176518077A>C , CM000667.1:g.176518077A>C	GRCh37
NC_000005.8:g.176450683A>C	NCBI36
NG_012067.1:g.9157A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.575A>C MANE Select	ENSP00000292408.4:p.His192Pro
ENST00000292408.8:c.575A>C	ENSP00000292408.4:p.His192Pro
ENST00000393637.5:c.575A>C	ENSP00000377254.1:p.His192Pro
ENST00000393648.6:c.575A>C	ENSP00000377259.2:p.His192Pro
ENST00000426612.5:n.692A>C
ENST00000430285.5:c.*439A>C	ENSP00000395164.1:n.*439A>C
ENST00000502906.5:c.575A>C	ENSP00000424960.1:p.His192Pro
ENST00000503708.5:c.575A>C	ENSP00000424905.1:p.His192Pro
ENST00000509511.5:n.575A>C
NM_001291980.1:c.575A>C	NP_001278909.1:p.His192Pro
NM_002011.4:c.575A>C	NP_002002.3:p.His192Pro
NM_022963.3:c.575A>C	NP_075252.2:p.His192Pro
NM_213647.2:c.575A>C	NP_998812.1:p.His192Pro
XM_005265838.2:c.575A>C	XP_005265895.1:p.His192Pro
XM_011534464.1:c.668A>C	XP_011532766.1:p.His223Pro
XM_011534465.1:c.257A>C	XP_011532767.1:p.His86Pro
XR_941090.1:n.620A>C
NM_001354984.1:c.575A>C	NP_001341913.1:p.His192Pro
NM_213647.3:c.575A>C MANE Select	NP_998812.1:p.His192Pro
NM_001291980.2:c.575A>C	NP_001278909.1:p.His192Pro
NM_001354984.2:c.575A>C	NP_001341913.1:p.His192Pro
NM_002011.5:c.575A>C	NP_002002.3:p.His192Pro