Canonical Allele Identifier: CA2676681036

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177091088-GCATTGGAGGCATTCGGGTGAGTCTCTGGGTTCCAAGACCGTCTGCTCCCCCATTTTCATTCCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177091092_177091155del , CM000667.2:g.177091092_177091155del	GRCh38
NC_000005.9:g.176518093_176518156del , CM000667.1:g.176518093_176518156del	GRCh37
NC_000005.8:g.176450699_176450762del	NCBI36
NG_012067.1:g.9173_9236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.591_603+51del
ENST00000292408.8:c.591_603+51del
ENST00000393637.5:c.591_603+51del
ENST00000393648.6:c.591_603+51del
ENST00000502906.5:c.591_603+51del
ENST00000509511.5:n.591_603+51del
NM_001291980.1:c.591_603+51del
NM_002011.4:c.591_603+51del
NM_022963.3:c.591_603+51del
NM_213647.2:c.591_603+51del
XM_005265838.2:c.591_603+51del
XM_011534464.1:c.684_696+51del
XM_011534465.1:c.273_285+51del
XR_941090.1:n.636_648+51del
NM_001354984.1:c.591_603+51del
NM_213647.3:c.591_603+51del
NM_001291980.2:c.591_603+51del
NM_001354984.2:c.591_603+51del
NM_002011.5:c.591_603+51del