Canonical Allele Identifier: CA362292846

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520428T>G (hg19) ; chr5:g.177093427T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093427T>G , CM000667.2:g.177093427T>G	GRCh38
NC_000005.9:g.176520428T>G , CM000667.1:g.176520428T>G	GRCh37
NC_000005.8:g.176453034T>G	NCBI36
NG_012067.1:g.11508T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1273T>G MANE Select	ENSP00000292408.4:p.Ser425Ala
ENST00000292408.8:c.1273T>G	ENSP00000292408.4:p.Ser425Ala
ENST00000393637.5:c.1153T>G	ENSP00000377254.1:p.Ser385Ala
ENST00000393648.6:c.1119T>G	ENSP00000377259.2:p.Leu373=
ENST00000502906.5:c.1273T>G	ENSP00000424960.1:p.Ser425Ala
ENST00000508139.1:n.651T>G
ENST00000511076.1:c.167T>G
NM_001291980.1:c.1119T>G	NP_001278909.1:p.Leu373=
NM_002011.4:c.1273T>G	NP_002002.3:p.Ser425Ala
NM_022963.3:c.1153T>G	NP_075252.2:p.Ser385Ala
NM_213647.2:c.1273T>G	NP_998812.1:p.Ser425Ala
XM_005265838.2:c.1273T>G	XP_005265895.1:p.Ser425Ala
XM_011534464.1:c.1366T>G	XP_011532766.1:p.Ser456Ala
XM_011534465.1:c.955T>G	XP_011532767.1:p.Ser319Ala
XR_941090.1:n.1318T>G
NM_001354984.1:c.1273T>G	NP_001341913.1:p.Ser425Ala
NM_213647.3:c.1273T>G MANE Select	NP_998812.1:p.Ser425Ala
NM_001291980.2:c.1119T>G	NP_001278909.1:p.Leu373=
NM_001354984.2:c.1273T>G	NP_001341913.1:p.Ser425Ala
NM_002011.5:c.1273T>G	NP_002002.3:p.Ser425Ala