Canonical Allele Identifier: CA2210125549
Gene: ABCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16142159T= , CM000678.2:g.16142159T= GRCh38
NC_000016.9:g.16236016T= , CM000678.1:g.16236016T= GRCh37
NC_000016.8:g.16143517T= NCBI36
NG_028268.1:g.197583T=
NG_028268.2:g.197583T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399408.7:c.*878T= ENSP00000382340.4:n.*878T=
ENST00000399410.8:c.*878T= MANE Select ENSP00000382342.3:n.*878T=
ENST00000572882.3:c.*878T= ENSP00000461615.2:n.*878T=
ENST00000676806.1:n.2200T=
ENST00000677164.1:c.*878T= ENSP00000502873.1:n.*878T=
ENST00000678422.1:c.*2571T= ENSP00000503954.1:n.*2571T=
ENST00000399408.6:c.*878T= ENSP00000382340.3:n.*878T=
ENST00000399410.7:c.*878T= ENSP00000382342.3:n.*878T=
NM_004996.3:c.*878T= NP_004987.2:n.*878T=
XM_011522497.1:c.*878T= XP_011520799.1:n.*878T=
XM_011522498.1:c.*878T= XP_011520800.1:n.*878T=
XM_011522498.2:c.*878T= XP_011520800.1:n.*878T=
XM_017023237.1:c.*878T= XP_016878726.1:n.*878T=
XM_017023238.1:c.*878T= XP_016878727.1:n.*878T=
XM_017023239.1:c.*878T= XP_016878728.1:n.*878T=
XM_017023240.1:c.*878T= XP_016878729.1:n.*878T=
XM_017023241.1:c.*878T= XP_016878730.1:n.*878T=
XM_017023242.1:c.*878T= XP_016878731.1:n.*878T=
NM_004996.4:c.*878T= MANE Select NP_004987.2:n.*878T=