Canonical Allele Identifier: CA2614740917

Gene: CPT1A

Linked Data

• gnomAD v4: 11-68759802-C-CCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68759802_68759803insCCA , CM000673.2:g.68759802_68759803insCCA	GRCh38
NC_000011.9:g.68527270_68527271insCCA , CM000673.1:g.68527270_68527271insCCA	GRCh37
NC_000011.8:g.68283846_68283847insCCA	NCBI36
NG_011801.1:g.87129_87130insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265641.10:c.2143-142_2143-141insTGG MANE Select	ENSP00000265641.4:n.2143-142_2143-141insTGG
ENST00000265641.9:c.2143-142_2143-141insTGG	ENSP00000265641.4:n.2143-142_2143-141insTGG
ENST00000376618.6:c.2143-142_2143-141insTGG	ENSP00000365803.2:n.2143-142_2143-141insTGG
ENST00000539743.5:c.2143-142_2143-141insTGG	ENSP00000446108.1:n.2143-142_2143-141insTGG
ENST00000540367.5:c.2143-142_2143-141insTGG	ENSP00000439084.1:n.2143-142_2143-141insTGG
NM_001031847.2:c.2143-142_2143-141insTGG	NP_001027017.1:n.2143-142_2143-141insTGG
NM_001876.3:c.2143-142_2143-141insTGG	NP_001867.2:n.2143-142_2143-141insTGG
XM_005273762.1:c.2239-142_2239-141insTGG	XP_005273819.1:n.2239-142_2239-141insTGG
XM_005273763.1:c.2239-142_2239-141insTGG	XP_005273820.1:n.2239-142_2239-141insTGG
XM_005273762.3:c.2239-142_2239-141insTGG	XP_005273819.1:n.2239-142_2239-141insTGG
XM_017017220.1:c.2143-142_2143-141insTGG	XP_016872709.1:n.2143-142_2143-141insTGG
NM_001876.4:c.2143-142_2143-141insTGG MANE Select	NP_001867.2:n.2143-142_2143-141insTGG
NM_001031847.3:c.2143-142_2143-141insTGG	NP_001027017.1:n.2143-142_2143-141insTGG