Canonical Allele Identifier: CA1490464396

Gene: FGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851350_122851352delinsCAA , CM000666.2:g.122851350_122851352delinsCAA	GRCh38
NC_000004.11:g.123772505_123772507delinsCAA , CM000666.1:g.123772505_123772507delinsCAA	GRCh37
NC_000004.10:g.123991955_123991957delinsCAA	NCBI36
NG_029067.1:g.29643_29645delinsCAA
NG_029067.2:g.29643_29645delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264498.9:c.577+23998_577+24000delinsCAA	ENSP00000264498.4:n.577+23998_577+24000delinsCAA
ENST00000264498.8:c.577+23998_577+24000delinsCAA	ENSP00000264498.4:n.577+23998_577+24000delinsCAA
ENST00000644866.2:c.178+23998_178+24000delinsCAA MANE Select	ENSP00000494222.1:n.178+23998_178+24000delinsCAA
ENST00000264498.7:c.577+23998_577+24000delinsCAA	ENSP00000264498.3:n.577+23998_577+24000delinsCAA
ENST00000608478.1:c.178+23998_178+24000delinsCAA	ENSP00000477134.1:n.178+23998_178+24000delinsCAA
ENST00000614010.4:c.577+23998_577+24000delinsCAA	ENSP00000478620.1:n.577+23998_577+24000delinsCAA
NM_002006.4:c.577+23998_577+24000delinsCAA	NP_001997.5:n.577+23998_577+24000delinsCAA
NM_001361665.1:c.178+23998_178+24000delinsCAA	NP_001348594.1:n.178+23998_178+24000delinsCAA
NM_002006.5:c.577+23998_577+24000delinsCAA	NP_001997.5:n.577+23998_577+24000delinsCAA
NM_001361665.2:c.178+23998_178+24000delinsCAA MANE Select	NP_001348594.1:n.178+23998_178+24000delinsCAA
NM_002006.6:c.577+23998_577+24000delinsCAA	NP_001997.5:n.577+23998_577+24000delinsCAA