Canonical Allele Identifier: CA2220670263
Gene: ABCC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.48146113T= , CM000678.2:g.48146113T= GRCh38
NC_000016.9:g.48180024T= , CM000678.1:g.48180024T= GRCh37
NC_000016.8:g.46737525T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000311303.8:c.119+193A= MANE Select ENSP00000311030.4:n.119+193A=
ENST00000528693.6:c.119+193A= ENSP00000510388.1:n.119+193A=
ENST00000532494.6:n.465+193A=
ENST00000311303.7:c.119+193A= ENSP00000311030.3:n.119+193A=
ENST00000497206.6:c.119+193A= ENSP00000431232.1:n.119+193A=
ENST00000527640.1:c.119+193A= ENSP00000436647.1:n.119+193A=
ENST00000528693.5:n.322+193A=
ENST00000529084.5:c.119+193A= ENSP00000434510.1:n.119+193A=
ENST00000529504.5:c.119+193A= ENSP00000433333.1:n.119+193A=
ENST00000532494.5:c.119+193A= ENSP00000437047.1:n.119+193A=
ENST00000533639.5:c.119+193A= ENSP00000435715.1:n.119+193A=
ENST00000534418.5:c.119+193A= ENSP00000431354.1:n.119+193A=
NM_033226.2:c.119+193A= NP_150229.2:n.119+193A=
NM_001392028.1:c.119+193A= NP_001378957.1:n.119+193A=
NM_001393797.1:c.119+193A= MANE Select NP_001380726.1:n.119+193A=
NM_033226.3:c.119+193A= NP_150229.2:n.119+193A=
NR_171628.1:n.591+193A=
NR_171629.1:n.169+193A=
NR_171630.1:n.169+193A=
NR_171631.1:n.169+193A=
NR_171632.1:n.169+193A=
NR_171633.1:n.169+193A=