Canonical Allele Identifier: CA447959166

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177097547-C-T
• MyVariant Identifiers: chr5:g.176524548C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097547C>T , CM000667.2:g.177097547C>T	GRCh38
NC_000005.9:g.176524548C>T , CM000667.1:g.176524548C>T	GRCh37
NC_000005.8:g.176457154C>T	NCBI36
NG_012067.1:g.15628C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.2280C>T MANE Select	ENSP00000292408.4:p.Thr760=
ENST00000292408.8:c.2280C>T	ENSP00000292408.4:p.Thr760=
ENST00000393637.5:c.2160C>T	ENSP00000377254.1:p.Thr720=
ENST00000393648.6:c.2076C>T	ENSP00000377259.2:p.Thr692=
ENST00000502906.5:c.2280C>T	ENSP00000424960.1:p.Thr760=
ENST00000513423.1:n.228C>T
NM_001291980.1:c.2076C>T	NP_001278909.1:p.Thr692=
NM_002011.4:c.2280C>T	NP_002002.3:p.Thr760=
NM_022963.3:c.2160C>T	NP_075252.2:p.Thr720=
NM_213647.2:c.2280C>T	NP_998812.1:p.Thr760=
XM_005265838.2:c.2280C>T	XP_005265895.1:p.Thr760=
XM_011534464.1:c.2373C>T	XP_011532766.1:p.Thr791=
XM_011534465.1:c.1962C>T	XP_011532767.1:p.Thr654=
NM_001354984.1:c.2280C>T	NP_001341913.1:p.Thr760=
NM_213647.3:c.2280C>T MANE Select	NP_998812.1:p.Thr760=
NM_001291980.2:c.2076C>T	NP_001278909.1:p.Thr692=
NM_001354984.2:c.2280C>T	NP_001341913.1:p.Thr760=
NM_002011.5:c.2280C>T	NP_002002.3:p.Thr760=