Canonical Allele Identifier: CA362299708

Gene: FGFR4

Linked Data

• MyVariant Identifiers: chr5:g.176524558T>C (hg19) ; chr5:g.177097557T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097557T>C , CM000667.2:g.177097557T>C	GRCh38
NC_000005.9:g.176524558T>C , CM000667.1:g.176524558T>C	GRCh37
NC_000005.8:g.176457164T>C	NCBI36
NG_012067.1:g.15638T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.2290T>C MANE Select	ENSP00000292408.4:p.Tyr764His
ENST00000292408.8:c.2290T>C	ENSP00000292408.4:p.Tyr764His
ENST00000393637.5:c.2170T>C	ENSP00000377254.1:p.Tyr724His
ENST00000393648.6:c.2086T>C	ENSP00000377259.2:p.Tyr696His
ENST00000502906.5:c.2290T>C	ENSP00000424960.1:p.Tyr764His
ENST00000513423.1:n.238T>C
NM_001291980.1:c.2086T>C	NP_001278909.1:p.Tyr696His
NM_002011.4:c.2290T>C	NP_002002.3:p.Tyr764His
NM_022963.3:c.2170T>C	NP_075252.2:p.Tyr724His
NM_213647.2:c.2290T>C	NP_998812.1:p.Tyr764His
XM_005265838.2:c.2290T>C	XP_005265895.1:p.Tyr764His
XM_011534464.1:c.2383T>C	XP_011532766.1:p.Tyr795His
XM_011534465.1:c.1972T>C	XP_011532767.1:p.Tyr658His
NM_001354984.1:c.2290T>C	NP_001341913.1:p.Tyr764His
NM_213647.3:c.2290T>C MANE Select	NP_998812.1:p.Tyr764His
NM_001291980.2:c.2086T>C	NP_001278909.1:p.Tyr696His
NM_001354984.2:c.2290T>C	NP_001341913.1:p.Tyr764His
NM_002011.5:c.2290T>C	NP_002002.3:p.Tyr764His