Canonical Allele Identifier: CA340393705

Gene: CPT2

Linked Data

• MyVariant Identifiers: chr1:g.53676131A>T (hg19) ; chr1:g.53210459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210459A>T , CM000663.2:g.53210459A>T	GRCh38
NC_000001.10:g.53676131A>T , CM000663.1:g.53676131A>T	GRCh37
NC_000001.9:g.53448719A>T	NCBI36
NG_008035.1:g.19031A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.785A>T MANE Select	ENSP00000360541.3:p.Asn262Ile
ENST00000635862.1:c.785A>T	ENSP00000490867.1:p.Asn262Ile
ENST00000635888.1:c.*771A>T	ENSP00000490042.1:n.*771A>T
ENST00000636239.1:c.*432A>T	ENSP00000490066.1:n.*432A>T
ENST00000636867.1:c.785A>T	ENSP00000489631.1:p.Asn262Ile
ENST00000636891.1:c.785A>T	ENSP00000490399.1:p.Asn262Ile
ENST00000636935.1:c.341-2805A>T	ENSP00000489757.1:n.341-2805A>T
ENST00000637252.1:c.785A>T	ENSP00000490492.1:p.Asn262Ile
ENST00000637726.1:n.2985A>T
ENST00000638135.1:c.*432A>T	ENSP00000489756.1:n.*432A>T
ENST00000371486.3:c.785A>T	ENSP00000360541.3:p.Asn262Ile
NM_000098.2:c.785A>T	NP_000089.1:p.Asn262Ile
XM_005270484.1:c.785A>T	XP_005270541.1:p.Asn262Ile
NM_001330589.1:c.785A>T	NP_001317518.1:p.Asn262Ile
NM_000098.3:c.785A>T MANE Select	NP_000089.1:p.Asn262Ile
NM_001330589.2:c.785A>T	NP_001317518.1:p.Asn262Ile