Canonical Allele Identifier: CA2002762146

Gene: APOA1 APOA1-AS

Linked Data

• dbSNP Id: rs1941556269

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116836580C>T , CM000673.2:g.116836580C>T	GRCh38
NC_000011.9:g.116707296C>T , CM000673.1:g.116707296C>T	GRCh37
NC_000011.8:g.116212506C>T	NCBI36
NG_012021.1:g.6043G>A , LRG_767:g.6043G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.201-169G>A (APOA1) MANE Select	ENSP00000236850.3:n.201-169G>A
ENST00000236850.4:c.201-169G>A (APOA1)	ENSP00000236850.3:n.201-169G>A
ENST00000359492.6:c.201-169G>A (APOA1)	ENSP00000352471.2:n.201-169G>A
ENST00000375320.5:c.201-169G>A (APOA1)	ENSP00000364469.1:n.201-169G>A
ENST00000375323.5:c.201-169G>A (APOA1)	ENSP00000364472.1:n.201-169G>A
ENST00000375329.6:c.135-169G>A (APOA1)	ENSP00000364478.2:n.135-169G>A
NM_000039.1:c.201-169G>A , LRG_767t1:c.201-169G>A (APOA1)	NP_000030.1:n.201-169G>A
NR_126362.1:n.123+341C>T (APOA1-AS)
XM_005271539.2:c.201-169G>A (APOA1)	XP_005271596.1:n.201-169G>A
XM_005271540.1:c.201-169G>A (APOA1)	XP_005271597.1:n.201-169G>A
NM_000039.2:c.201-169G>A (APOA1)	NP_000030.1:n.201-169G>A
NM_001318017.1:c.201-169G>A (APOA1)	NP_001304946.1:n.201-169G>A
NM_001318018.1:c.201-169G>A (APOA1)	NP_001304947.1:n.201-169G>A
NM_001318021.1:c.-127-169G>A (APOA1)	NP_001304950.1:n.-127-169G>A
NM_001318017.2:c.201-169G>A (APOA1)	NP_001304946.1:n.201-169G>A
NM_001318018.2:c.201-169G>A (APOA1)	NP_001304947.1:n.201-169G>A
NM_000039.3:c.201-169G>A (APOA1) MANE Select	NP_000030.1:n.201-169G>A