Canonical Allele Identifier: CA1167208830
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196773A= , CM000663.2:g.53196773A= GRCh38
NC_000001.10:g.53662445A= , CM000663.1:g.53662445A= GRCh37
NC_000001.9:g.53435033A= NCBI36
NG_008035.1:g.5345A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-171A= ENSP00000360541.3:n.-171A=
NM_000098.2:c.-171A= NP_000089.1:n.-171A=
XM_005270484.1:c.-171A= XP_005270541.1:n.-171A=
NM_001330589.1:c.-171A= NP_001317518.1:n.-171A=