Canonical Allele Identifier: CA340393775

Gene: CPT2

Linked Data

• MyVariant Identifiers: chr1:g.53676151A>T (hg19) ; chr1:g.53210479A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210479A>T , CM000663.2:g.53210479A>T	GRCh38
NC_000001.10:g.53676151A>T , CM000663.1:g.53676151A>T	GRCh37
NC_000001.9:g.53448739A>T	NCBI36
NG_008035.1:g.19051A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.805A>T MANE Select	ENSP00000360541.3:p.Ile269Phe
ENST00000635862.1:c.805A>T	ENSP00000490867.1:p.Ile269Phe
ENST00000635888.1:c.*791A>T	ENSP00000490042.1:n.*791A>T
ENST00000636239.1:c.*452A>T	ENSP00000490066.1:n.*452A>T
ENST00000636867.1:c.805A>T	ENSP00000489631.1:p.Ile269Phe
ENST00000636891.1:c.805A>T	ENSP00000490399.1:p.Ile269Phe
ENST00000636935.1:c.341-2785A>T	ENSP00000489757.1:n.341-2785A>T
ENST00000637252.1:c.805A>T	ENSP00000490492.1:p.Ile269Phe
ENST00000637726.1:n.3005A>T
ENST00000638135.1:c.*452A>T	ENSP00000489756.1:n.*452A>T
ENST00000371486.3:c.805A>T	ENSP00000360541.3:p.Ile269Phe
NM_000098.2:c.805A>T	NP_000089.1:p.Ile269Phe
XM_005270484.1:c.805A>T	XP_005270541.1:p.Ile269Phe
NM_001330589.1:c.805A>T	NP_001317518.1:p.Ile269Phe
NM_000098.3:c.805A>T MANE Select	NP_000089.1:p.Ile269Phe
NM_001330589.2:c.805A>T	NP_001317518.1:p.Ile269Phe