Canonical Allele Identifier: CA2461235255
Gene: FGF13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139035154G= , CM000685.2:g.139035154G= GRCh38
NC_000023.10:g.138117316G= , CM000685.1:g.138117316G= GRCh37
NC_000023.9:g.137944982G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000436198.6:c.49+168905C= ENSP00000396198.2:n.49+168905C=
ENST00000441825.8:c.-148-44537C= ENSP00000409276.2:n.-148-44537C=
ENST00000421460.1:c.-113+168262C= ENSP00000388688.1:n.-113+168262C=
ENST00000436198.5:c.49+168905C= ENSP00000396198.2:n.49+168905C=
ENST00000448673.1:c.49+168905C= ENSP00000411999.1:n.49+168905C=
ENST00000626909.2:c.49+168905C= ENSP00000487411.1:n.49+168905C=
NM_001139498.1:c.49+168905C= NP_001132970.1:n.49+168905C=
NM_001139500.1:c.49+168905C= NP_001132972.1:n.49+168905C=
NM_001139501.1:c.-148-44537C= NP_001132973.1:n.-148-44537C=
XM_005262399.1:c.49+168905C= XP_005262456.1:n.49+168905C=
XM_011531315.1:c.82+168262C= XP_011529617.1:n.82+168262C=
XM_024452352.1:c.82+168262C= XP_024308120.1:n.82+168262C=
NM_001139498.2:c.49+168905C= NP_001132970.1:n.49+168905C=
NM_001139500.2:c.49+168905C= NP_001132972.1:n.49+168905C=
NM_001139501.2:c.-148-44537C= NP_001132973.1:n.-148-44537C=