Canonical Allele Identifier: CA340392718
Gene: CPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53210243G>C , CM000663.2:g.53210243G>C GRCh38
NC_000001.10:g.53675915G>C , CM000663.1:g.53675915G>C GRCh37
NC_000001.9:g.53448503G>C NCBI36
NG_008035.1:g.18815G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.4:c.569G>C MANE Select ENSP00000360541.3:p.Arg190Thr
ENST00000635862.1:c.569G>C ENSP00000490867.1:p.Arg190Thr
ENST00000635888.1:c.*555G>C ENSP00000490042.1:n.*555G>C
ENST00000636239.1:c.*216G>C ENSP00000490066.1:n.*216G>C
ENST00000636867.1:c.569G>C ENSP00000489631.1:p.Arg190Thr
ENST00000636891.1:c.569G>C ENSP00000490399.1:p.Arg190Thr
ENST00000636935.1:c.341-3021G>C ENSP00000489757.1:n.341-3021G>C
ENST00000637252.1:c.569G>C ENSP00000490492.1:p.Arg190Thr
ENST00000637726.1:n.2769G>C
ENST00000638135.1:c.*216G>C ENSP00000489756.1:n.*216G>C
ENST00000371486.3:c.569G>C ENSP00000360541.3:p.Arg190Thr
NM_000098.2:c.569G>C NP_000089.1:p.Arg190Thr
XM_005270484.1:c.569G>C XP_005270541.1:p.Arg190Thr
NM_001330589.1:c.569G>C NP_001317518.1:p.Arg190Thr
NM_000098.3:c.569G>C MANE Select NP_000089.1:p.Arg190Thr
NM_001330589.2:c.569G>C NP_001317518.1:p.Arg190Thr