Canonical Allele Identifier: CA2676682295

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093536-AGTTCCCCCGGGACAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093539_177093553del , CM000667.2:g.177093539_177093553del	GRCh38
NC_000005.9:g.176520540_176520554del , CM000667.1:g.176520540_176520554del	GRCh37
NC_000005.8:g.176453146_176453160del	NCBI36
NG_012067.1:g.11620_11634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1385_1397+2del
ENST00000292408.8:c.1385_1397+2del
ENST00000393637.5:c.1265_1277+2del
ENST00000393648.6:c.1193+38_1193+52del	ENSP00000377259.2:n.1193+38_1193+52del
ENST00000502906.5:c.1385_1397+2del
ENST00000511076.1:c.279_291+2del
NM_001291980.1:c.1193+38_1193+52del	NP_001278909.1:n.1193+38_1193+52del
NM_002011.4:c.1385_1397+2del
NM_022963.3:c.1265_1277+2del
NM_213647.2:c.1385_1397+2del
XM_005265838.2:c.1385_1397+2del
XM_011534464.1:c.1478_1490+2del
XM_011534465.1:c.1067_1079+2del
XR_941090.1:n.1392+38_1392+52del
NM_001354984.1:c.1385_1397+2del
NM_213647.3:c.1385_1397+2del
NM_001291980.2:c.1193+38_1193+52del	NP_001278909.1:n.1193+38_1193+52del
NM_001354984.2:c.1385_1397+2del
NM_002011.5:c.1385_1397+2del