Canonical Allele Identifier: CA363426866

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657236T>C , CM000668.2:g.31657236T>C GRCh38
NC_000006.11:g.31625013T>C , CM000668.1:g.31625013T>C GRCh37
NC_000006.10:g.31732992T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.281T>C (APOM) MANE Select ENSP00000365081.3:p.Leu94Pro
ENST00000375916.3:c.281T>C (APOM) ENSP00000365081.3:p.Leu94Pro
ENST00000375918.6:c.65T>C (APOM) ENSP00000365083.2:p.Leu22Pro
ENST00000375920.8:c.65T>C (APOM) ENSP00000365085.4:p.Leu22Pro
NM_001256169.1:c.65T>C (APOM) NP_001243098.1:p.Leu22Pro
NM_019101.2:c.281T>C (APOM) NP_061974.2:p.Leu94Pro
NR_045828.1:n.316T>C (APOM)
XM_006715150.2:c.185T>C (APOM) XP_006715213.1:p.Leu62Pro
XM_011514895.1:c.-14+3085A>G (BAG6) XP_011513197.1:n.-14+3085A>G
XM_006715150.3:c.185T>C (APOM) XP_006715213.1:p.Leu62Pro
XM_017011279.2:c.-14+3085A>G (BAG6) XP_016866768.1:n.-14+3085A>G
XM_024446545.1:c.-14+528A>G (BAG6) XP_024302313.1:n.-14+528A>G
NM_019101.3:c.281T>C (APOM) MANE Select NP_061974.2:p.Leu94Pro
NM_001256169.2:c.65T>C (APOM) NP_001243098.1:p.Leu22Pro
NR_045828.2:n.322T>C (APOM)