Canonical Allele Identifier: CA363427538

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625175C>G (hg19) ; chr6:g.31657398C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657398C>G , CM000668.2:g.31657398C>G	GRCh38
NC_000006.11:g.31625175C>G , CM000668.1:g.31625175C>G	GRCh37
NC_000006.10:g.31733154C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.362C>G (APOM) MANE Select	ENSP00000365081.3:p.Thr121Ser
ENST00000375916.3:c.362C>G (APOM)	ENSP00000365081.3:p.Thr121Ser
ENST00000375918.6:c.146C>G (APOM)	ENSP00000365083.2:p.Thr49Ser
ENST00000375920.8:c.146C>G (APOM)	ENSP00000365085.4:p.Thr49Ser
NM_001256169.1:c.146C>G (APOM)	NP_001243098.1:p.Thr49Ser
NM_019101.2:c.362C>G (APOM)	NP_061974.2:p.Thr121Ser
NR_045828.1:n.397C>G (APOM)
XM_006715150.2:c.266C>G (APOM)	XP_006715213.1:p.Thr89Ser
XM_011514895.1:c.-14+2923G>C (BAG6)	XP_011513197.1:n.-14+2923G>C
XM_006715150.3:c.266C>G (APOM)	XP_006715213.1:p.Thr89Ser
XM_017011279.2:c.-14+2923G>C (BAG6)	XP_016866768.1:n.-14+2923G>C
XM_024446545.1:c.-14+366G>C (BAG6)	XP_024302313.1:n.-14+366G>C
NM_019101.3:c.362C>G (APOM) MANE Select	NP_061974.2:p.Thr121Ser
NM_001256169.2:c.146C>G (APOM)	NP_001243098.1:p.Thr49Ser
NR_045828.2:n.403C>G (APOM)