Canonical Allele Identifier: CA362293137

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176520469C>T (hg19) ; chr5:g.177093468C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093468C>T , CM000667.2:g.177093468C>T	GRCh38
NC_000005.9:g.176520469C>T , CM000667.1:g.176520469C>T	GRCh37
NC_000005.8:g.176453075C>T	NCBI36
NG_012067.1:g.11549C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1314C>T MANE Select	ENSP00000292408.4:p.Leu438=
ENST00000292408.8:c.1314C>T	ENSP00000292408.4:p.Leu438=
ENST00000393637.5:c.1194C>T	ENSP00000377254.1:p.Leu398=
ENST00000393648.6:c.1160C>T	ENSP00000377259.2:p.Ser387Phe
ENST00000502906.5:c.1314C>T	ENSP00000424960.1:p.Leu438=
ENST00000508139.1:n.692C>T
ENST00000511076.1:c.208C>T
NM_001291980.1:c.1160C>T	NP_001278909.1:p.Ser387Phe
NM_002011.4:c.1314C>T	NP_002002.3:p.Leu438=
NM_022963.3:c.1194C>T	NP_075252.2:p.Leu398=
NM_213647.2:c.1314C>T	NP_998812.1:p.Leu438=
XM_005265838.2:c.1314C>T	XP_005265895.1:p.Leu438=
XM_011534464.1:c.1407C>T	XP_011532766.1:p.Leu469=
XM_011534465.1:c.996C>T	XP_011532767.1:p.Leu332=
XR_941090.1:n.1359C>T
NM_001354984.1:c.1314C>T	NP_001341913.1:p.Leu438=
NM_213647.3:c.1314C>T MANE Select	NP_998812.1:p.Leu438=
NM_001291980.2:c.1160C>T	NP_001278909.1:p.Ser387Phe
NM_001354984.2:c.1314C>T	NP_001341913.1:p.Leu438=
NM_002011.5:c.1314C>T	NP_002002.3:p.Leu438=