Canonical Allele Identifier: CA362286941

Gene: FGFR4

Linked Data

• dbSNP Id: rs2149731898
• gnomAD v4: 5-177090994-G-T
• MyVariant Identifiers: chr5:g.176517995G>T (hg19) ; chr5:g.177090994G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090994G>T , CM000667.2:g.177090994G>T	GRCh38
NC_000005.9:g.176517995G>T , CM000667.1:g.176517995G>T	GRCh37
NC_000005.8:g.176450601G>T	NCBI36
NG_012067.1:g.9075G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.493G>T MANE Select	ENSP00000292408.4:p.Gly165Trp
ENST00000292408.8:c.493G>T	ENSP00000292408.4:p.Gly165Trp
ENST00000393637.5:c.493G>T	ENSP00000377254.1:p.Gly165Trp
ENST00000393648.6:c.493G>T	ENSP00000377259.2:p.Gly165Trp
ENST00000426612.5:n.610G>T
ENST00000430285.5:c.*357G>T	ENSP00000395164.1:n.*357G>T
ENST00000502906.5:c.493G>T	ENSP00000424960.1:p.Gly165Trp
ENST00000503708.5:c.493G>T	ENSP00000424905.1:p.Gly165Trp
ENST00000509511.5:n.493G>T
NM_001291980.1:c.493G>T	NP_001278909.1:p.Gly165Trp
NM_002011.4:c.493G>T	NP_002002.3:p.Gly165Trp
NM_022963.3:c.493G>T	NP_075252.2:p.Gly165Trp
NM_213647.2:c.493G>T	NP_998812.1:p.Gly165Trp
XM_005265838.2:c.493G>T	XP_005265895.1:p.Gly165Trp
XM_011534464.1:c.586G>T	XP_011532766.1:p.Gly196Trp
XM_011534465.1:c.175G>T	XP_011532767.1:p.Gly59Trp
XR_941090.1:n.538G>T
NM_001354984.1:c.493G>T	NP_001341913.1:p.Gly165Trp
NM_213647.3:c.493G>T MANE Select	NP_998812.1:p.Gly165Trp
NM_001291980.2:c.493G>T	NP_001278909.1:p.Gly165Trp
NM_001354984.2:c.493G>T	NP_001341913.1:p.Gly165Trp
NM_002011.5:c.493G>T	NP_002002.3:p.Gly165Trp