Canonical Allele Identifier: CA1167208703
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs746815144

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196595_53196596dup , CM000663.2:g.53196595_53196596dup GRCh38
NC_000001.10:g.53662267_53662268dup , CM000663.1:g.53662267_53662268dup GRCh37
NC_000001.9:g.53434855_53434856dup NCBI36
NG_008035.1:g.5167_5168dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-349_-348dup ENSP00000360541.3:n.-349_-348dup
NM_000098.2:c.-349_-348dup NP_000089.1:n.-349_-348dup
NM_001330589.1:c.-349_-348dup NP_001317518.1:n.-349_-348dup