Canonical Allele Identifier: CA417874904

Gene: CPT2

Linked Data

• ClinVar Variation Id: 1104046
• ClinVar RCV Id: RCV001427971
• dbSNP Id: rs1438452698
• MyVariant Identifiers: chr1:g.53676309A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210637A>G , CM000663.2:g.53210637A>G	GRCh38
NC_000001.10:g.53676309A>G , CM000663.1:g.53676309A>G	GRCh37
NC_000001.9:g.53448897A>G	NCBI36
NG_008035.1:g.19209A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.963A>G MANE Select	ENSP00000360541.3:p.Ala321=
ENST00000635862.1:c.963A>G	ENSP00000490867.1:p.Ala321=
ENST00000635888.1:c.*949A>G	ENSP00000490042.1:n.*949A>G
ENST00000636239.1:c.*610A>G	ENSP00000490066.1:n.*610A>G
ENST00000636867.1:c.963A>G	ENSP00000489631.1:p.Ala321=
ENST00000636891.1:c.963A>G	ENSP00000490399.1:p.Ala321=
ENST00000636935.1:c.341-2627A>G	ENSP00000489757.1:n.341-2627A>G
ENST00000637252.1:c.963A>G	ENSP00000490492.1:p.Ala321=
ENST00000637726.1:n.3163A>G
ENST00000638135.1:c.*610A>G	ENSP00000489756.1:n.*610A>G
ENST00000371486.3:c.963A>G	ENSP00000360541.3:p.Ala321=
NM_000098.2:c.963A>G	NP_000089.1:p.Ala321=
XM_005270484.1:c.963A>G	XP_005270541.1:p.Ala321=
NM_001330589.1:c.963A>G	NP_001317518.1:p.Ala321=
NM_000098.3:c.963A>G MANE Select	NP_000089.1:p.Ala321=
NM_001330589.2:c.963A>G	NP_001317518.1:p.Ala321=