Canonical Allele Identifier: CA564490396

Gene: FGFR4

Linked Data

• dbSNP Id: rs1270233320
• gnomAD v2: 5-176519628-AGCAT-A
• gnomAD v3: 5-177092627-AGCAT-A
• gnomAD v4: 5-177092627-AGCAT-A
• MyVariant Identifiers: chr5:g.176519629_176519632del (hg19) ; chr5:g.177092628_177092631del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177092629_177092632del , CM000667.2:g.177092629_177092632del	GRCh38
NC_000005.9:g.176519630_176519633del , CM000667.1:g.176519630_176519633del	GRCh37
NC_000005.8:g.176452236_176452239del	NCBI36
NG_012067.1:g.10710_10713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.919-17_919-14del MANE Select	ENSP00000292408.4:n.919-17_919-14del
ENST00000292408.8:c.919-17_919-14del	ENSP00000292408.4:n.919-17_919-14del
ENST00000393637.5:c.919-17_919-14del	ENSP00000377254.1:n.919-17_919-14del
ENST00000393648.6:c.919-17_919-14del	ENSP00000377259.2:n.919-17_919-14del
ENST00000502906.5:c.919-17_919-14del	ENSP00000424960.1:n.919-17_919-14del
ENST00000508139.1:n.223-17_223-14del
ENST00000509511.5:n.919-17_919-14del
NM_001291980.1:c.919-17_919-14del	NP_001278909.1:n.919-17_919-14del
NM_002011.4:c.919-17_919-14del	NP_002002.3:n.919-17_919-14del
NM_022963.3:c.919-17_919-14del	NP_075252.2:n.919-17_919-14del
NM_213647.2:c.919-17_919-14del	NP_998812.1:n.919-17_919-14del
XM_005265838.2:c.919-17_919-14del	XP_005265895.1:n.919-17_919-14del
XM_011534464.1:c.1012-17_1012-14del	XP_011532766.1:n.1012-17_1012-14del
XM_011534465.1:c.601-17_601-14del	XP_011532767.1:n.601-17_601-14del
XR_941090.1:n.964-17_964-14del
NM_001354984.1:c.919-17_919-14del	NP_001341913.1:n.919-17_919-14del
NM_213647.3:c.919-17_919-14del MANE Select	NP_998812.1:n.919-17_919-14del
NM_001291980.2:c.919-17_919-14del	NP_001278909.1:n.919-17_919-14del
NM_001354984.2:c.919-17_919-14del	NP_001341913.1:n.919-17_919-14del
NM_002011.5:c.919-17_919-14del	NP_002002.3:n.919-17_919-14del