Canonical Allele Identifier: CA477048614

Gene: APOA1

Linked Data

• MyVariant Identifiers: chr11:g.116706692T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116835976T>C , CM000673.2:g.116835976T>C	GRCh38
NC_000011.9:g.116706692T>C , CM000673.1:g.116706692T>C	GRCh37
NC_000011.8:g.116211902T>C	NCBI36
NG_012021.1:g.6647A>G , LRG_767:g.6647A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236850.5:c.636A>G MANE Select	ENSP00000236850.3:p.Arg212=
ENST00000236850.4:c.636A>G	ENSP00000236850.3:p.Arg212=
ENST00000359492.6:c.636A>G	ENSP00000352471.2:p.Arg212=
ENST00000375320.5:c.636A>G	ENSP00000364469.1:p.Arg212=
ENST00000375323.5:c.636A>G	ENSP00000364472.1:p.Arg212=
ENST00000375329.6:c.570A>G	ENSP00000364478.2:p.Arg190=
NM_000039.1:c.636A>G , LRG_767t1:c.636A>G	NP_000030.1:p.Arg212=
XM_005271539.2:c.636A>G	XP_005271596.1:p.Arg212=
XM_005271540.1:c.636A>G	XP_005271597.1:p.Arg212=
NM_000039.2:c.636A>G	NP_000030.1:p.Arg212=
NM_001318017.1:c.636A>G	NP_001304946.1:p.Arg212=
NM_001318018.1:c.636A>G	NP_001304947.1:p.Arg212=
NM_001318021.1:c.309A>G	NP_001304950.1:p.Arg103=
NM_001318017.2:c.636A>G	NP_001304946.1:p.Arg212=
NM_001318018.2:c.636A>G	NP_001304947.1:p.Arg212=
NM_000039.3:c.636A>G MANE Select	NP_000030.1:p.Arg212=