Canonical Allele Identifier: CA2210069757
Gene: ABCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2048693984

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16034842_16034850del , CM000678.2:g.16034842_16034850del GRCh38
NC_000016.9:g.16128699_16128707del , CM000678.1:g.16128699_16128707del GRCh37
NC_000016.8:g.16036200_16036208del NCBI36
NG_028268.1:g.90266_90274del
NG_028268.2:g.90266_90274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.678-1630_678-1622del ENSP00000382340.4:n.678-1630_678-1622del
ENST00000399410.8:c.678-1630_678-1622del MANE Select ENSP00000382342.3:n.678-1630_678-1622del
ENST00000572882.3:c.678-1630_678-1622del ENSP00000461615.2:n.678-1630_678-1622del
ENST00000574224.2:n.753-1630_753-1622del
ENST00000677164.1:c.552-1630_552-1622del ENSP00000502873.1:n.552-1630_552-1622del
ENST00000678422.1:c.678-1630_678-1622del ENSP00000503954.1:n.678-1630_678-1622del
ENST00000679043.1:n.630-1630_630-1622del
ENST00000399408.6:c.-301-1630_-301-1622del ENSP00000382340.3:n.-301-1630_-301-1622del
ENST00000399410.7:c.678-1630_678-1622del ENSP00000382342.3:n.678-1630_678-1622del
ENST00000572882.2:c.373-1630_373-1622del
ENST00000574224.1:n.278-1630_278-1622del
NM_004996.3:c.678-1630_678-1622del NP_004987.2:n.678-1630_678-1622del
XM_011522497.1:c.654-1630_654-1622del XP_011520799.1:n.654-1630_654-1622del
XM_011522498.1:c.732-1630_732-1622del XP_011520800.1:n.732-1630_732-1622del
XM_011522498.2:c.732-1630_732-1622del XP_011520800.1:n.732-1630_732-1622del
XM_017023237.1:c.732-1630_732-1622del XP_016878726.1:n.732-1630_732-1622del
XM_017023238.1:c.606-1630_606-1622del XP_016878727.1:n.606-1630_606-1622del
XM_017023239.1:c.594-1630_594-1622del XP_016878728.1:n.594-1630_594-1622del
XM_017023240.1:c.732-1630_732-1622del XP_016878729.1:n.732-1630_732-1622del
XM_017023241.1:c.468-1630_468-1622del XP_016878730.1:n.468-1630_468-1622del
XM_017023242.1:c.732-1630_732-1622del XP_016878731.1:n.732-1630_732-1622del
XM_017023243.2:c.732-1630_732-1622del XP_016878732.1:n.732-1630_732-1622del
NM_004996.4:c.678-1630_678-1622del MANE Select NP_004987.2:n.678-1630_678-1622del