Canonical Allele Identifier: CA2210069756
Gene: ABCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16034839_16034848delinsCAGCCTCCCA , CM000678.2:g.16034839_16034848delinsCAGCCTCCCA GRCh38
NC_000016.9:g.16128696_16128705delinsCAGCCTCCCA , CM000678.1:g.16128696_16128705delinsCAGCCTCCCA GRCh37
NC_000016.8:g.16036197_16036206delinsCAGCCTCCCA NCBI36
NG_028268.1:g.90263_90272delinsCAGCCTCCCA
NG_028268.2:g.90263_90272delinsCAGCCTCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.678-1633_678-1624delinsCAGCCTCCCA ENSP00000382340.4:n.678-1633_678-1624delinsCAGCCTCCCA
ENST00000399410.8:c.678-1633_678-1624delinsCAGCCTCCCA MANE Select ENSP00000382342.3:n.678-1633_678-1624delinsCAGCCTCCCA
ENST00000572882.3:c.678-1633_678-1624delinsCAGCCTCCCA ENSP00000461615.2:n.678-1633_678-1624delinsCAGCCTCCCA
ENST00000574224.2:n.753-1633_753-1624delinsCAGCCTCCCA
ENST00000677164.1:c.552-1633_552-1624delinsCAGCCTCCCA ENSP00000502873.1:n.552-1633_552-1624delinsCAGCCTCCCA
ENST00000678422.1:c.678-1633_678-1624delinsCAGCCTCCCA ENSP00000503954.1:n.678-1633_678-1624delinsCAGCCTCCCA
ENST00000679043.1:n.630-1633_630-1624delinsCAGCCTCCCA
ENST00000399408.6:c.-301-1633_-301-1624delinsCAGCCTCCCA ENSP00000382340.3:n.-301-1633_-301-1624delinsCAGCCTCCCA
ENST00000399410.7:c.678-1633_678-1624delinsCAGCCTCCCA ENSP00000382342.3:n.678-1633_678-1624delinsCAGCCTCCCA
ENST00000572882.2:c.373-1633_373-1624delinsCAGCCTCCCA
ENST00000574224.1:n.278-1633_278-1624delinsCAGCCTCCCA
NM_004996.3:c.678-1633_678-1624delinsCAGCCTCCCA NP_004987.2:n.678-1633_678-1624delinsCAGCCTCCCA
XM_011522497.1:c.654-1633_654-1624delinsCAGCCTCCCA XP_011520799.1:n.654-1633_654-1624delinsCAGCCTCCCA
XM_011522498.1:c.732-1633_732-1624delinsCAGCCTCCCA XP_011520800.1:n.732-1633_732-1624delinsCAGCCTCCCA
XM_011522498.2:c.732-1633_732-1624delinsCAGCCTCCCA XP_011520800.1:n.732-1633_732-1624delinsCAGCCTCCCA
XM_017023237.1:c.732-1633_732-1624delinsCAGCCTCCCA XP_016878726.1:n.732-1633_732-1624delinsCAGCCTCCCA
XM_017023238.1:c.606-1633_606-1624delinsCAGCCTCCCA XP_016878727.1:n.606-1633_606-1624delinsCAGCCTCCCA
XM_017023239.1:c.594-1633_594-1624delinsCAGCCTCCCA XP_016878728.1:n.594-1633_594-1624delinsCAGCCTCCCA
XM_017023240.1:c.732-1633_732-1624delinsCAGCCTCCCA XP_016878729.1:n.732-1633_732-1624delinsCAGCCTCCCA
XM_017023241.1:c.468-1633_468-1624delinsCAGCCTCCCA XP_016878730.1:n.468-1633_468-1624delinsCAGCCTCCCA
XM_017023242.1:c.732-1633_732-1624delinsCAGCCTCCCA XP_016878731.1:n.732-1633_732-1624delinsCAGCCTCCCA
XM_017023243.2:c.732-1633_732-1624delinsCAGCCTCCCA XP_016878732.1:n.732-1633_732-1624delinsCAGCCTCCCA
NM_004996.4:c.678-1633_678-1624delinsCAGCCTCCCA MANE Select NP_004987.2:n.678-1633_678-1624delinsCAGCCTCCCA