Canonical Allele Identifier: CA3576245

Gene: FGFR4

Linked Data

• dbSNP Id: rs766515277
• ExAC: 5:176520054 GGAGGGACT / G
• gnomAD v2: 5-176520054-GGAGGGACT-G
• gnomAD v4: 5-177093053-GGAGGGACT-G
• MyVariant Identifiers: chr5:g.176520055_176520062del (hg19) ; chr5:g.177093054_177093061del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093057_177093064del , CM000667.2:g.177093057_177093064del	GRCh38
NC_000005.9:g.176520058_176520065del , CM000667.1:g.176520058_176520065del	GRCh37
NC_000005.8:g.176452664_176452671del	NCBI36
NG_012067.1:g.11138_11145del

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1058-81_1058-74del MANE Select	ENSP00000292408.4:n.1058-81_1058-74del
ENST00000292408.8:c.1058-81_1058-74del	ENSP00000292408.4:n.1058-81_1058-74del
ENST00000393637.5:c.1057+273_1058-268del	ENSP00000377254.1:n.1057+273_1058-268del
ENST00000393648.6:c.1058-81_1058-74del	ENSP00000377259.2:n.1058-81_1058-74del
ENST00000502906.5:c.1058-81_1058-74del	ENSP00000424960.1:n.1058-81_1058-74del
ENST00000508139.1:n.362-81_362-74del
ENST00000509511.5:n.1330_1337del
NM_001291980.1:c.1058-81_1058-74del	NP_001278909.1:n.1058-81_1058-74del
NM_002011.4:c.1058-81_1058-74del	NP_002002.3:n.1058-81_1058-74del
NM_022963.3:c.1057+273_1058-268del	NP_075252.2:n.1057+273_1058-268del
NM_213647.2:c.1058-81_1058-74del	NP_998812.1:n.1058-81_1058-74del
XM_005265838.2:c.1058-81_1058-74del	XP_005265895.1:n.1058-81_1058-74del
XM_011534464.1:c.1151-81_1151-74del	XP_011532766.1:n.1151-81_1151-74del
XM_011534465.1:c.740-81_740-74del	XP_011532767.1:n.740-81_740-74del
XR_941090.1:n.1103-81_1103-74del
NM_001354984.1:c.1058-81_1058-74del	NP_001341913.1:n.1058-81_1058-74del
NM_213647.3:c.1058-81_1058-74del MANE Select	NP_998812.1:n.1058-81_1058-74del
NM_001291980.2:c.1058-81_1058-74del	NP_001278909.1:n.1058-81_1058-74del
NM_001354984.2:c.1058-81_1058-74del	NP_001341913.1:n.1058-81_1058-74del
NM_002011.5:c.1058-81_1058-74del	NP_002002.3:n.1058-81_1058-74del