Canonical Allele Identifier: CA340393991

Gene: CPT2

Linked Data

• MyVariant Identifiers: chr1:g.53676211G>A (hg19) ; chr1:g.53210539G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210539G>A , CM000663.2:g.53210539G>A	GRCh38
NC_000001.10:g.53676211G>A , CM000663.1:g.53676211G>A	GRCh37
NC_000001.9:g.53448799G>A	NCBI36
NG_008035.1:g.19111G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371486.4:c.865G>A MANE Select	ENSP00000360541.3:p.Ala289Thr
ENST00000635862.1:c.865G>A	ENSP00000490867.1:p.Ala289Thr
ENST00000635888.1:c.*851G>A	ENSP00000490042.1:n.*851G>A
ENST00000636239.1:c.*512G>A	ENSP00000490066.1:n.*512G>A
ENST00000636867.1:c.865G>A	ENSP00000489631.1:p.Ala289Thr
ENST00000636891.1:c.865G>A	ENSP00000490399.1:p.Ala289Thr
ENST00000636935.1:c.341-2725G>A	ENSP00000489757.1:n.341-2725G>A
ENST00000637252.1:c.865G>A	ENSP00000490492.1:p.Ala289Thr
ENST00000637726.1:n.3065G>A
ENST00000638135.1:c.*512G>A	ENSP00000489756.1:n.*512G>A
ENST00000371486.3:c.865G>A	ENSP00000360541.3:p.Ala289Thr
NM_000098.2:c.865G>A	NP_000089.1:p.Ala289Thr
XM_005270484.1:c.865G>A	XP_005270541.1:p.Ala289Thr
NM_001330589.1:c.865G>A	NP_001317518.1:p.Ala289Thr
NM_000098.3:c.865G>A MANE Select	NP_000089.1:p.Ala289Thr
NM_001330589.2:c.865G>A	NP_001317518.1:p.Ala289Thr