Canonical Allele Identifier: CA22639808

Gene: CPT2

Linked Data

• ClinVar Variation Id: 1020752
• ClinVar RCV Id: RCV001320383 ; RCV002486273 ; RCV003456216 ; RCV003449913 ; RCV003449914 ; RCV003449915
• dbSNP Id: rs992811256
• gnomAD v4: 1-53211098-T-A
• MyVariant Identifiers: chr1:g.53676770T>A (hg19) ; chr1:g.53211098T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53211098T>A , CM000663.2:g.53211098T>A	GRCh38
NC_000001.10:g.53676770T>A , CM000663.1:g.53676770T>A	GRCh37
NC_000001.9:g.53449358T>A	NCBI36
NG_008035.1:g.19670T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1424T>A MANE Select	ENSP00000360541.3:p.Phe475Tyr
ENST00000635862.1:c.1424T>A	ENSP00000490867.1:p.Phe475Tyr
ENST00000635888.1:c.*1410T>A	ENSP00000490042.1:n.*1410T>A
ENST00000636239.1:c.*1071T>A	ENSP00000490066.1:n.*1071T>A
ENST00000636867.1:c.1424T>A	ENSP00000489631.1:p.Phe475Tyr
ENST00000636891.1:c.1424T>A	ENSP00000490399.1:p.Phe475Tyr
ENST00000636935.1:c.341-2166T>A	ENSP00000489757.1:n.341-2166T>A
ENST00000637252.1:c.1424T>A	ENSP00000490492.1:p.Phe475Tyr
ENST00000637726.1:n.3624T>A
ENST00000638135.1:c.*1071T>A	ENSP00000489756.1:n.*1071T>A
ENST00000371486.3:c.1424T>A	ENSP00000360541.3:p.Phe475Tyr
NM_000098.2:c.1424T>A	NP_000089.1:p.Phe475Tyr
XM_005270484.1:c.1424T>A	XP_005270541.1:p.Phe475Tyr
NM_001330589.1:c.1424T>A	NP_001317518.1:p.Phe475Tyr
NM_000098.3:c.1424T>A MANE Select	NP_000089.1:p.Phe475Tyr
NM_001330589.2:c.1424T>A	NP_001317518.1:p.Phe475Tyr