Canonical Allele Identifier: CA3000195488
Gene: ABCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16016430dup , CM000678.2:g.16016430dup GRCh38
NC_000016.9:g.16110287dup , CM000678.1:g.16110287dup GRCh37
NC_000016.8:g.16017788dup NCBI36
NG_028268.1:g.71854dup
NG_028268.2:g.71854dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.490-66dup ENSP00000382340.4:n.490-66dup
ENST00000399410.8:c.490-66dup MANE Select ENSP00000382342.3:n.490-66dup
ENST00000572882.3:c.490-66dup ENSP00000461615.2:n.490-66dup
ENST00000574224.2:n.565-66dup
ENST00000677164.1:c.489+1802dup ENSP00000502873.1:n.489+1802dup
ENST00000678422.1:c.490-66dup ENSP00000503954.1:n.490-66dup
ENST00000679043.1:n.442-66dup
ENST00000399408.6:c.-489-66dup ENSP00000382340.3:n.-489-66dup
ENST00000399410.7:c.490-66dup ENSP00000382342.3:n.490-66dup
ENST00000572882.2:c.185-66dup
ENST00000574224.1:n.90-66dup
NM_004996.3:c.490-66dup NP_004987.2:n.490-66dup
XM_011522497.1:c.466-66dup XP_011520799.1:n.466-66dup
XM_011522498.1:c.544-66dup XP_011520800.1:n.544-66dup
XM_011522498.2:c.544-66dup XP_011520800.1:n.544-66dup
XM_017023237.1:c.544-66dup XP_016878726.1:n.544-66dup
XM_017023238.1:c.543+1802dup XP_016878727.1:n.543+1802dup
XM_017023239.1:c.406-66dup XP_016878728.1:n.406-66dup
XM_017023240.1:c.544-66dup XP_016878729.1:n.544-66dup
XM_017023241.1:c.405+6529dup XP_016878730.1:n.405+6529dup
XM_017023242.1:c.544-66dup XP_016878731.1:n.544-66dup
XM_017023243.2:c.544-66dup XP_016878732.1:n.544-66dup
NM_004996.4:c.490-66dup MANE Select NP_004987.2:n.490-66dup