Canonical Allele Identifier: CA2645706481
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196814-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196814G>A , CM000663.2:g.53196814G>A GRCh38
NC_000001.10:g.53662486G>A , CM000663.1:g.53662486G>A GRCh37
NC_000001.9:g.53435074G>A NCBI36
NG_008035.1:g.5386G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636239.1:c.-130G>A ENSP00000490066.1:n.-130G>A
ENST00000636867.1:c.-130G>A ENSP00000489631.1:n.-130G>A
ENST00000636891.1:c.-130G>A ENSP00000490399.1:n.-130G>A
ENST00000636935.1:c.-130G>A ENSP00000489757.1:n.-130G>A
ENST00000637252.1:c.-130G>A ENSP00000490492.1:n.-130G>A
ENST00000371486.3:c.-130G>A ENSP00000360541.3:n.-130G>A
NM_000098.2:c.-130G>A NP_000089.1:n.-130G>A
XM_005270484.1:c.-130G>A XP_005270541.1:n.-130G>A
NM_001330589.1:c.-130G>A NP_001317518.1:n.-130G>A
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