Canonical Allele Identifier: CA362292402

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093359-G-T
• MyVariant Identifiers: chr5:g.176520360G>T (hg19) ; chr5:g.177093359G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093359G>T , CM000667.2:g.177093359G>T	GRCh38
NC_000005.9:g.176520360G>T , CM000667.1:g.176520360G>T	GRCh37
NC_000005.8:g.176452966G>T	NCBI36
NG_012067.1:g.11440G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1251+28G>T MANE Select	ENSP00000292408.4:n.1251+28G>T
ENST00000292408.8:c.1251+28G>T	ENSP00000292408.4:n.1251+28G>T
ENST00000393637.5:c.1085G>T	ENSP00000377254.1:p.Cys362Phe
ENST00000393648.6:c.1098-47G>T	ENSP00000377259.2:n.1098-47G>T
ENST00000502906.5:c.1251+28G>T	ENSP00000424960.1:n.1251+28G>T
ENST00000508139.1:n.583G>T
ENST00000511076.1:c.157+28G>T
NM_001291980.1:c.1098-47G>T	NP_001278909.1:n.1098-47G>T
NM_002011.4:c.1251+28G>T	NP_002002.3:n.1251+28G>T
NM_022963.3:c.1085G>T	NP_075252.2:p.Cys362Phe
NM_213647.2:c.1251+28G>T	NP_998812.1:n.1251+28G>T
XM_005265838.2:c.1251+28G>T	XP_005265895.1:n.1251+28G>T
XM_011534464.1:c.1344+28G>T	XP_011532766.1:n.1344+28G>T
XM_011534465.1:c.933+28G>T	XP_011532767.1:n.933+28G>T
XR_941090.1:n.1296+28G>T
NM_001354984.1:c.1251+28G>T	NP_001341913.1:n.1251+28G>T
NM_213647.3:c.1251+28G>T MANE Select	NP_998812.1:n.1251+28G>T
NM_001291980.2:c.1098-47G>T	NP_001278909.1:n.1098-47G>T
NM_001354984.2:c.1251+28G>T	NP_001341913.1:n.1251+28G>T
NM_002011.5:c.1251+28G>T	NP_002002.3:n.1251+28G>T