Canonical Allele Identifier: CA2676681069

Gene: FGFR4

Linked Data

• dbSNP Id: rs1273489530
• gnomAD v4: 5-177091149-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091149C>A , CM000667.2:g.177091149C>A	GRCh38
NC_000005.9:g.176518150C>A , CM000667.1:g.176518150C>A	GRCh37
NC_000005.8:g.176450756C>A	NCBI36
NG_012067.1:g.9230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.603+45C>A MANE Select	ENSP00000292408.4:n.603+45C>A
ENST00000292408.8:c.603+45C>A	ENSP00000292408.4:n.603+45C>A
ENST00000393637.5:c.603+45C>A	ENSP00000377254.1:n.603+45C>A
ENST00000393648.6:c.603+45C>A	ENSP00000377259.2:n.603+45C>A
ENST00000502906.5:c.603+45C>A	ENSP00000424960.1:n.603+45C>A
ENST00000509511.5:n.603+45C>A
NM_001291980.1:c.603+45C>A	NP_001278909.1:n.603+45C>A
NM_002011.4:c.603+45C>A	NP_002002.3:n.603+45C>A
NM_022963.3:c.603+45C>A	NP_075252.2:n.603+45C>A
NM_213647.2:c.603+45C>A	NP_998812.1:n.603+45C>A
XM_005265838.2:c.603+45C>A	XP_005265895.1:n.603+45C>A
XM_011534464.1:c.696+45C>A	XP_011532766.1:n.696+45C>A
XM_011534465.1:c.285+45C>A	XP_011532767.1:n.285+45C>A
XR_941090.1:n.648+45C>A
NM_001354984.1:c.603+45C>A	NP_001341913.1:n.603+45C>A
NM_213647.3:c.603+45C>A MANE Select	NP_998812.1:n.603+45C>A
NM_001291980.2:c.603+45C>A	NP_001278909.1:n.603+45C>A
NM_001354984.2:c.603+45C>A	NP_001341913.1:n.603+45C>A
NM_002011.5:c.603+45C>A	NP_002002.3:n.603+45C>A