Canonical Allele Identifier: CA1167208859
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196806C= , CM000663.2:g.53196806C= GRCh38
NC_000001.10:g.53662478C= , CM000663.1:g.53662478C= GRCh37
NC_000001.9:g.53435066C= NCBI36
NG_008035.1:g.5378C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636239.1:c.-138C= ENSP00000490066.1:n.-138C=
ENST00000636867.1:c.-138C= ENSP00000489631.1:n.-138C=
ENST00000636891.1:c.-138C= ENSP00000490399.1:n.-138C=
ENST00000637252.1:c.-138C= ENSP00000490492.1:n.-138C=
ENST00000371486.3:c.-138C= ENSP00000360541.3:n.-138C=
NM_000098.2:c.-138C= NP_000089.1:n.-138C=
XM_005270484.1:c.-138C= XP_005270541.1:n.-138C=
NM_001330589.1:c.-138C= NP_001317518.1:n.-138C=