Canonical Allele Identifier: CA2210121674
Gene: ABCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16134399_16134400delinsGC , CM000678.2:g.16134399_16134400delinsGC GRCh38
NC_000016.9:g.16228256_16228257delinsGC , CM000678.1:g.16228256_16228257delinsGC GRCh37
NC_000016.8:g.16135757_16135758delinsGC NCBI36
NG_028268.1:g.189823_189824delinsGC
NG_028268.2:g.189823_189824delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.4046_4047delinsGC ENSP00000382340.4:p.Gly1349=
ENST00000399410.8:c.4016_4017delinsGC MANE Select ENSP00000382342.3:p.Gly1339=
ENST00000572882.3:c.3839_3840delinsGC ENSP00000461615.2:p.Gly1280=
ENST00000676806.1:n.742_743delinsGC
ENST00000677164.1:c.3545_3546delinsGC ENSP00000502873.1:p.Gly1182=
ENST00000678422.1:c.*1308_*1309delinsGC ENSP00000503954.1:n.*1308_*1309delinsGC
ENST00000399408.6:c.3068_3069delinsGC ENSP00000382340.3:p.Gly1023=
ENST00000399410.7:c.4016_4017delinsGC ENSP00000382342.3:p.Gly1339=
ENST00000572882.2:c.3741_3742delinsGC
NM_004996.3:c.4016_4017delinsGC NP_004987.2:p.Gly1339=
XM_011522497.1:c.3992_3993delinsGC XP_011520799.1:p.Gly1331=
XM_011522498.1:c.3923_3924delinsGC XP_011520800.1:p.Gly1308=
XM_011522498.2:c.3923_3924delinsGC XP_011520800.1:p.Gly1308=
XM_017023237.1:c.4070_4071delinsGC XP_016878726.1:p.Gly1357=
XM_017023238.1:c.3944_3945delinsGC XP_016878727.1:p.Gly1315=
XM_017023239.1:c.3932_3933delinsGC XP_016878728.1:p.Gly1311=
XM_017023240.1:c.3893_3894delinsGC XP_016878729.1:p.Gly1298=
XM_017023241.1:c.3806_3807delinsGC XP_016878730.1:p.Gly1269=
XM_017023242.1:c.3725_3726delinsGC XP_016878731.1:p.Gly1242=
NM_004996.4:c.4016_4017delinsGC MANE Select NP_004987.2:p.Gly1339=