Canonical Allele Identifier: CA2210035897
Gene: ABCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.15955776T>A , CM000678.2:g.15955776T>A GRCh38
NC_000016.9:g.16049633T>A , CM000678.1:g.16049633T>A GRCh37
NC_000016.8:g.15957134T>A NCBI36
NG_028268.1:g.11200T>A
NG_028268.2:g.11200T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.48+5977T>A ENSP00000382340.4:n.48+5977T>A
ENST00000399410.8:c.48+5977T>A MANE Select ENSP00000382342.3:n.48+5977T>A
ENST00000572882.3:c.48+5977T>A ENSP00000461615.2:n.48+5977T>A
ENST00000574224.2:n.123+6516T>A
ENST00000677164.1:c.48+5977T>A ENSP00000502873.1:n.48+5977T>A
ENST00000678422.1:c.48+5977T>A ENSP00000503954.1:n.48+5977T>A
ENST00000399408.6:c.-931+5977T>A ENSP00000382340.3:n.-931+5977T>A
ENST00000399410.7:c.48+5977T>A ENSP00000382342.3:n.48+5977T>A
NM_004996.3:c.48+5977T>A NP_004987.2:n.48+5977T>A
NM_004996.4:c.48+5977T>A MANE Select NP_004987.2:n.48+5977T>A