Canonical Allele Identifier: CA340396903

Gene: CPT2

Linked Data

• gnomAD v4: 1-53211269-T-C
• MyVariant Identifiers: chr1:g.53676941T>C (hg19) ; chr1:g.53211269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53211269T>C , CM000663.2:g.53211269T>C	GRCh38
NC_000001.10:g.53676941T>C , CM000663.1:g.53676941T>C	GRCh37
NC_000001.9:g.53449529T>C	NCBI36
NG_008035.1:g.19841T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1595T>C MANE Select	ENSP00000360541.3:p.Met532Thr
ENST00000635862.1:c.1576+19T>C	ENSP00000490867.1:n.1576+19T>C
ENST00000635888.1:c.*1581T>C	ENSP00000490042.1:n.*1581T>C
ENST00000636239.1:c.*1242T>C	ENSP00000490066.1:n.*1242T>C
ENST00000636867.1:c.1576+19T>C	ENSP00000489631.1:n.1576+19T>C
ENST00000636891.1:c.1595T>C	ENSP00000490399.1:p.Met532Thr
ENST00000636935.1:c.341-1995T>C	ENSP00000489757.1:n.341-1995T>C
ENST00000637252.1:c.1595T>C	ENSP00000490492.1:p.Met532Thr
ENST00000637726.1:n.3795T>C
ENST00000638135.1:c.*1242T>C	ENSP00000489756.1:n.*1242T>C
ENST00000371486.3:c.1595T>C	ENSP00000360541.3:p.Met532Thr
NM_000098.2:c.1595T>C	NP_000089.1:p.Met532Thr
XM_005270484.1:c.1576+19T>C	XP_005270541.1:n.1576+19T>C
NM_001330589.1:c.1576+19T>C	NP_001317518.1:n.1576+19T>C
NM_000098.3:c.1595T>C MANE Select	NP_000089.1:p.Met532Thr
NM_001330589.2:c.1576+19T>C	NP_001317518.1:n.1576+19T>C