Canonical Allele Identifier: CA347805

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210126G>A , CM000663.2:g.53210126G>A	GRCh38
NC_000001.10:g.53675798G>A , CM000663.1:g.53675798G>A	GRCh37
NC_000001.9:g.53448386G>A	NCBI36
NG_008035.1:g.18698G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.452G>A MANE Select	ENSP00000360541.3:p.Arg151Gln
ENST00000635862.1:c.452G>A	ENSP00000490867.1:p.Arg151Gln
ENST00000635888.1:c.*438G>A	ENSP00000490042.1:n.*438G>A
ENST00000636239.1:c.*99G>A	ENSP00000490066.1:n.*99G>A
ENST00000636867.1:c.452G>A	ENSP00000489631.1:p.Arg151Gln
ENST00000636891.1:c.452G>A	ENSP00000490399.1:p.Arg151Gln
ENST00000636935.1:c.341-3138G>A	ENSP00000489757.1:n.341-3138G>A
ENST00000637252.1:c.452G>A	ENSP00000490492.1:p.Arg151Gln
ENST00000637726.1:n.2652G>A
ENST00000638135.1:c.*99G>A	ENSP00000489756.1:n.*99G>A
ENST00000371486.3:c.452G>A	ENSP00000360541.3:p.Arg151Gln
NM_000098.2:c.452G>A	NP_000089.1:p.Arg151Gln
XM_005270484.1:c.452G>A	XP_005270541.1:p.Arg151Gln
NM_001330589.1:c.452G>A	NP_001317518.1:p.Arg151Gln
NM_000098.3:c.452G>A MANE Select	NP_000089.1:p.Arg151Gln
NM_001330589.2:c.452G>A	NP_001317518.1:p.Arg151Gln