Canonical Allele Identifier: CA340394048

Gene: CPT2

Linked Data

• ClinVar Variation Id: 570807
• ClinVar RCV Id: RCV000691762
• dbSNP Id: rs764849762
• MyVariant Identifiers: chr1:g.53676233G>C (hg19) ; chr1:g.53210561G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210561G>C , CM000663.2:g.53210561G>C	GRCh38
NC_000001.10:g.53676233G>C , CM000663.1:g.53676233G>C	GRCh37
NC_000001.9:g.53448821G>C	NCBI36
NG_008035.1:g.19133G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.887G>C MANE Select	ENSP00000360541.3:p.Arg296Pro
ENST00000635862.1:c.887G>C	ENSP00000490867.1:p.Arg296Pro
ENST00000635888.1:c.*873G>C	ENSP00000490042.1:n.*873G>C
ENST00000636239.1:c.*534G>C	ENSP00000490066.1:n.*534G>C
ENST00000636867.1:c.887G>C	ENSP00000489631.1:p.Arg296Pro
ENST00000636891.1:c.887G>C	ENSP00000490399.1:p.Arg296Pro
ENST00000636935.1:c.341-2703G>C	ENSP00000489757.1:n.341-2703G>C
ENST00000637252.1:c.887G>C	ENSP00000490492.1:p.Arg296Pro
ENST00000637726.1:n.3087G>C
ENST00000638135.1:c.*534G>C	ENSP00000489756.1:n.*534G>C
ENST00000371486.3:c.887G>C	ENSP00000360541.3:p.Arg296Pro
NM_000098.2:c.887G>C	NP_000089.1:p.Arg296Pro
XM_005270484.1:c.887G>C	XP_005270541.1:p.Arg296Pro
NM_001330589.1:c.887G>C	NP_001317518.1:p.Arg296Pro
NM_000098.3:c.887G>C MANE Select	NP_000089.1:p.Arg296Pro
NM_001330589.2:c.887G>C	NP_001317518.1:p.Arg296Pro