Canonical Allele Identifier: CA3576246

Gene: FGFR4

Linked Data

• dbSNP Id: rs776683021
• ExAC: 5:176520056 AGGGACTGAGTTAGGGT / A
• gnomAD v2: 5-176520056-AGGGACTGAGTTAGGGT-A
• gnomAD v4: 5-177093055-AGGGACTGAGTTAGGGT-A
• MyVariant Identifiers: chr5:g.176520057_176520072del (hg19) ; chr5:g.177093056_177093071del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093057_177093072del , CM000667.2:g.177093057_177093072del	GRCh38
NC_000005.9:g.176520058_176520073del , CM000667.1:g.176520058_176520073del	GRCh37
NC_000005.8:g.176452664_176452679del	NCBI36
NG_012067.1:g.11138_11153del

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.1058-81_1058-66del MANE Select	ENSP00000292408.4:n.1058-81_1058-66del
ENST00000292408.8:c.1058-81_1058-66del	ENSP00000292408.4:n.1058-81_1058-66del
ENST00000393637.5:c.1057+273_1058-260del	ENSP00000377254.1:n.1057+273_1058-260del
ENST00000393648.6:c.1058-81_1058-66del	ENSP00000377259.2:n.1058-81_1058-66del
ENST00000502906.5:c.1058-81_1058-66del	ENSP00000424960.1:n.1058-81_1058-66del
ENST00000508139.1:n.362-81_362-66del
NM_001291980.1:c.1058-81_1058-66del	NP_001278909.1:n.1058-81_1058-66del
NM_002011.4:c.1058-81_1058-66del	NP_002002.3:n.1058-81_1058-66del
NM_022963.3:c.1057+273_1058-260del	NP_075252.2:n.1057+273_1058-260del
NM_213647.2:c.1058-81_1058-66del	NP_998812.1:n.1058-81_1058-66del
XM_005265838.2:c.1058-81_1058-66del	XP_005265895.1:n.1058-81_1058-66del
XM_011534464.1:c.1151-81_1151-66del	XP_011532766.1:n.1151-81_1151-66del
XM_011534465.1:c.740-81_740-66del	XP_011532767.1:n.740-81_740-66del
XR_941090.1:n.1103-81_1103-66del
NM_001354984.1:c.1058-81_1058-66del	NP_001341913.1:n.1058-81_1058-66del
NM_213647.3:c.1058-81_1058-66del MANE Select	NP_998812.1:n.1058-81_1058-66del
NM_001291980.2:c.1058-81_1058-66del	NP_001278909.1:n.1058-81_1058-66del
NM_001354984.2:c.1058-81_1058-66del	NP_001341913.1:n.1058-81_1058-66del
NM_002011.5:c.1058-81_1058-66del	NP_002002.3:n.1058-81_1058-66del