Canonical Allele Identifier: CA2676681086

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177091172-ACAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091175_177091178del , CM000667.2:g.177091175_177091178del	GRCh38
NC_000005.9:g.176518176_176518179del , CM000667.1:g.176518176_176518179del	GRCh37
NC_000005.8:g.176450782_176450785del	NCBI36
NG_012067.1:g.9256_9259del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.603+71_603+74del MANE Select	ENSP00000292408.4:n.603+71_603+74del
ENST00000292408.8:c.603+71_603+74del	ENSP00000292408.4:n.603+71_603+74del
ENST00000393637.5:c.603+71_603+74del	ENSP00000377254.1:n.603+71_603+74del
ENST00000393648.6:c.603+71_603+74del	ENSP00000377259.2:n.603+71_603+74del
ENST00000502906.5:c.603+71_603+74del	ENSP00000424960.1:n.603+71_603+74del
ENST00000509511.5:n.603+71_603+74del
NM_001291980.1:c.603+71_603+74del	NP_001278909.1:n.603+71_603+74del
NM_002011.4:c.603+71_603+74del	NP_002002.3:n.603+71_603+74del
NM_022963.3:c.603+71_603+74del	NP_075252.2:n.603+71_603+74del
NM_213647.2:c.603+71_603+74del	NP_998812.1:n.603+71_603+74del
XM_005265838.2:c.603+71_603+74del	XP_005265895.1:n.603+71_603+74del
XM_011534464.1:c.696+71_696+74del	XP_011532766.1:n.696+71_696+74del
XM_011534465.1:c.285+71_285+74del	XP_011532767.1:n.285+71_285+74del
XR_941090.1:n.648+71_648+74del
NM_001354984.1:c.603+71_603+74del	NP_001341913.1:n.603+71_603+74del
NM_213647.3:c.603+71_603+74del MANE Select	NP_998812.1:n.603+71_603+74del
NM_001291980.2:c.603+71_603+74del	NP_001278909.1:n.603+71_603+74del
NM_001354984.2:c.603+71_603+74del	NP_001341913.1:n.603+71_603+74del
NM_002011.5:c.603+71_603+74del	NP_002002.3:n.603+71_603+74del