Canonical Allele Identifier: CA1619250613

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657193T= , CM000668.2:g.31657193T= GRCh38
NC_000006.11:g.31624970T= , CM000668.1:g.31624970T= GRCh37
NC_000006.10:g.31732949T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-32T= (APOM) MANE Select ENSP00000365081.3:n.270-32T=
ENST00000375916.3:c.270-32T= (APOM) ENSP00000365081.3:n.270-32T=
ENST00000375918.6:c.54-32T= (APOM) ENSP00000365083.2:n.54-32T=
ENST00000375920.8:c.54-32T= (APOM) ENSP00000365085.4:n.54-32T=
NM_001256169.1:c.54-32T= (APOM) NP_001243098.1:n.54-32T=
NM_019101.2:c.270-32T= (APOM) NP_061974.2:n.270-32T=
NR_045828.1:n.305-32T= (APOM)
XM_006715150.2:c.174-32T= (APOM) XP_006715213.1:n.174-32T=
XM_011514895.1:c.-14+3128A= (BAG6) XP_011513197.1:n.-14+3128A=
XM_006715150.3:c.174-32T= (APOM) XP_006715213.1:n.174-32T=
XM_017011279.2:c.-14+3128A= (BAG6) XP_016866768.1:n.-14+3128A=
XM_024446545.1:c.-14+571A= (BAG6) XP_024302313.1:n.-14+571A=
NM_019101.3:c.270-32T= (APOM) MANE Select NP_061974.2:n.270-32T=
NM_001256169.2:c.54-32T= (APOM) NP_001243098.1:n.54-32T=
NR_045828.2:n.311-32T= (APOM)