Canonical Allele Identifier: CA2574903287

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68784807_68784812dup , CM000673.2:g.68784807_68784812dup	GRCh38
NC_000011.9:g.68552275_68552280dup , CM000673.1:g.68552275_68552280dup	GRCh37
NC_000011.8:g.68308851_68308856dup	NCBI36
NG_011801.1:g.62120_62125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.1163+3_1163+8dup MANE Select	ENSP00000265641.4:n.1163+3_1163+8dup
ENST00000265641.9:c.1163+3_1163+8dup	ENSP00000265641.4:n.1163+3_1163+8dup
ENST00000376618.6:c.1163+3_1163+8dup	ENSP00000365803.2:n.1163+3_1163+8dup
ENST00000539743.5:c.1163+3_1163+8dup	ENSP00000446108.1:n.1163+3_1163+8dup
ENST00000540367.5:c.1163+3_1163+8dup	ENSP00000439084.1:n.1163+3_1163+8dup
NM_001031847.2:c.1163+3_1163+8dup	NP_001027017.1:n.1163+3_1163+8dup
NM_001876.3:c.1163+3_1163+8dup	NP_001867.2:n.1163+3_1163+8dup
XM_005273762.1:c.1259+3_1259+8dup	XP_005273819.1:n.1259+3_1259+8dup
XM_005273763.1:c.1259+3_1259+8dup	XP_005273820.1:n.1259+3_1259+8dup
XM_005273762.3:c.1259+3_1259+8dup	XP_005273819.1:n.1259+3_1259+8dup
XM_017017220.1:c.1163+3_1163+8dup	XP_016872709.1:n.1163+3_1163+8dup
NM_001876.4:c.1163+3_1163+8dup MANE Select	NP_001867.2:n.1163+3_1163+8dup
NM_001031847.3:c.1163+3_1163+8dup	NP_001027017.1:n.1163+3_1163+8dup