Canonical Allele Identifier: CA736855636

Gene: CPT2

Linked Data

• dbSNP Id: rs1478175298
• gnomAD v3: 1-53213179-T-C
• gnomAD v4: 1-53213179-T-C
• MyVariant Identifiers: chr1:g.53678851T>C (hg19) ; chr1:g.53213179T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53213179T>C , CM000663.2:g.53213179T>C	GRCh38
NC_000001.10:g.53678851T>C , CM000663.1:g.53678851T>C	GRCh37
NC_000001.9:g.53451439T>C	NCBI36
NG_008035.1:g.21751T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1646-85T>C MANE Select	ENSP00000360541.3:n.1646-85T>C
ENST00000635862.1:c.1613-85T>C	ENSP00000490867.1:n.1613-85T>C
ENST00000635888.1:c.*1632-85T>C	ENSP00000490042.1:n.*1632-85T>C
ENST00000636239.1:c.*1293-85T>C	ENSP00000490066.1:n.*1293-85T>C
ENST00000636867.1:c.1577-85T>C	ENSP00000489631.1:n.1577-85T>C
ENST00000636891.1:c.1696-85T>C	ENSP00000490399.1:n.1696-85T>C
ENST00000636935.1:c.341-85T>C	ENSP00000489757.1:n.341-85T>C
ENST00000637252.1:c.1682-85T>C	ENSP00000490492.1:n.1682-85T>C
ENST00000638135.1:c.*1293-85T>C	ENSP00000489756.1:n.*1293-85T>C
ENST00000371486.3:c.1646-85T>C	ENSP00000360541.3:n.1646-85T>C
NM_000098.2:c.1646-85T>C	NP_000089.1:n.1646-85T>C
XM_005270484.1:c.1577-85T>C	XP_005270541.1:n.1577-85T>C
NM_001330589.1:c.1577-85T>C	NP_001317518.1:n.1577-85T>C
NM_000098.3:c.1646-85T>C MANE Select	NP_000089.1:n.1646-85T>C
NM_001330589.2:c.1577-85T>C	NP_001317518.1:n.1577-85T>C