Canonical Allele Identifier: CA2461235272
Gene: FGF13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139035207C= , CM000685.2:g.139035207C= GRCh38
NC_000023.10:g.138117369C= , CM000685.1:g.138117369C= GRCh37
NC_000023.9:g.137945035C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000436198.6:c.49+168852G= ENSP00000396198.2:n.49+168852G=
ENST00000441825.8:c.-148-44590G= ENSP00000409276.2:n.-148-44590G=
ENST00000421460.1:c.-113+168209G= ENSP00000388688.1:n.-113+168209G=
ENST00000436198.5:c.49+168852G= ENSP00000396198.2:n.49+168852G=
ENST00000448673.1:c.49+168852G= ENSP00000411999.1:n.49+168852G=
ENST00000626909.2:c.49+168852G= ENSP00000487411.1:n.49+168852G=
NM_001139498.1:c.49+168852G= NP_001132970.1:n.49+168852G=
NM_001139500.1:c.49+168852G= NP_001132972.1:n.49+168852G=
NM_001139501.1:c.-148-44590G= NP_001132973.1:n.-148-44590G=
XM_005262399.1:c.49+168852G= XP_005262456.1:n.49+168852G=
XM_011531315.1:c.82+168209G= XP_011529617.1:n.82+168209G=
XM_024452352.1:c.82+168209G= XP_024308120.1:n.82+168209G=
NM_001139498.2:c.49+168852G= NP_001132970.1:n.49+168852G=
NM_001139500.2:c.49+168852G= NP_001132972.1:n.49+168852G=
NM_001139501.2:c.-148-44590G= NP_001132973.1:n.-148-44590G=