Canonical Allele Identifier: CA1490464389

Gene: FGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122851331_122851332delinsAT , CM000666.2:g.122851331_122851332delinsAT	GRCh38
NC_000004.11:g.123772486_123772487delinsAT , CM000666.1:g.123772486_123772487delinsAT	GRCh37
NC_000004.10:g.123991936_123991937delinsAT	NCBI36
NG_029067.1:g.29624_29625delinsAT
NG_029067.2:g.29624_29625delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264498.9:c.577+23979_577+23980delinsAT	ENSP00000264498.4:n.577+23979_577+23980delinsAT
ENST00000264498.8:c.577+23979_577+23980delinsAT	ENSP00000264498.4:n.577+23979_577+23980delinsAT
ENST00000644866.2:c.178+23979_178+23980delinsAT MANE Select	ENSP00000494222.1:n.178+23979_178+23980delinsAT
ENST00000264498.7:c.577+23979_577+23980delinsAT	ENSP00000264498.3:n.577+23979_577+23980delinsAT
ENST00000608478.1:c.178+23979_178+23980delinsAT	ENSP00000477134.1:n.178+23979_178+23980delinsAT
ENST00000614010.4:c.577+23979_577+23980delinsAT	ENSP00000478620.1:n.577+23979_577+23980delinsAT
NM_002006.4:c.577+23979_577+23980delinsAT	NP_001997.5:n.577+23979_577+23980delinsAT
NM_001361665.1:c.178+23979_178+23980delinsAT	NP_001348594.1:n.178+23979_178+23980delinsAT
NM_002006.5:c.577+23979_577+23980delinsAT	NP_001997.5:n.577+23979_577+23980delinsAT
NM_001361665.2:c.178+23979_178+23980delinsAT MANE Select	NP_001348594.1:n.178+23979_178+23980delinsAT
NM_002006.6:c.577+23979_577+23980delinsAT	NP_001997.5:n.577+23979_577+23980delinsAT