Canonical Allele Identifier: CA2631958639
Gene: ABCC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16142154del , CM000678.2:g.16142154del GRCh38
NC_000016.9:g.16236011del , CM000678.1:g.16236011del GRCh37
NC_000016.8:g.16143512del NCBI36
NG_028268.1:g.197578del
NG_028268.2:g.197578del

Transcript Alleles

HGVS Amino-acid change
ENST00000399408.7:c.*873del ENSP00000382340.4:n.*873del
ENST00000399410.8:c.*873del MANE Select ENSP00000382342.3:n.*873del
ENST00000572882.3:c.*873del ENSP00000461615.2:n.*873del
ENST00000676806.1:n.2195del
ENST00000677164.1:c.*873del ENSP00000502873.1:n.*873del
ENST00000678422.1:c.*2566del ENSP00000503954.1:n.*2566del
ENST00000399408.6:c.*873del ENSP00000382340.3:n.*873del
ENST00000399410.7:c.*873del ENSP00000382342.3:n.*873del
NM_004996.3:c.*873del NP_004987.2:n.*873del
XM_011522497.1:c.*873del XP_011520799.1:n.*873del
XM_011522498.1:c.*873del XP_011520800.1:n.*873del
XM_011522498.2:c.*873del XP_011520800.1:n.*873del
XM_017023237.1:c.*873del XP_016878726.1:n.*873del
XM_017023238.1:c.*873del XP_016878727.1:n.*873del
XM_017023239.1:c.*873del XP_016878728.1:n.*873del
XM_017023240.1:c.*873del XP_016878729.1:n.*873del
XM_017023241.1:c.*873del XP_016878730.1:n.*873del
XM_017023242.1:c.*873del XP_016878731.1:n.*873del
NM_004996.4:c.*873del MANE Select NP_004987.2:n.*873del