Canonical Allele Identifier: CA2390736110
Gene: ABCG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42296723G= , CM000683.2:g.42296723G= GRCh38
NC_000021.8:g.43716833G= , CM000683.1:g.43716833G= GRCh37
NC_000021.7:g.42589902G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398449.8:c.*331G= MANE Select ENSP00000381467.3:n.*331G=
ENST00000343687.7:c.*331G= ENSP00000339744.3:n.*331G=
ENST00000347800.6:c.*331G= ENSP00000291524.4:n.*331G=
ENST00000361802.6:c.*331G= ENSP00000354995.2:n.*331G=
ENST00000398437.1:c.*331G= ENSP00000381464.1:n.*331G=
ENST00000398449.7:c.*331G= ENSP00000381467.3:n.*331G=
ENST00000398457.6:c.*331G= ENSP00000381475.2:n.*331G=
ENST00000462050.5:n.2516G=
ENST00000472587.5:n.2382G=
NM_004915.3:c.*331G= NP_004906.3:n.*331G=
NM_016818.2:c.*331G= NP_058198.2:n.*331G=
NM_207174.1:c.*331G= NP_997057.1:n.*331G=
NM_207627.1:c.*331G= NP_997510.1:n.*331G=
NM_207628.1:c.*331G= NP_997511.1:n.*331G=
NM_207629.1:c.*331G= NP_997512.1:n.*331G=
XM_011529806.1:c.*331G= XP_011528108.1:n.*331G=
XM_011529807.1:c.*497G= XP_011528109.1:n.*497G=
XM_011529807.3:c.*497G= XP_011528109.1:n.*497G=
XM_024452141.1:c.*331G= XP_024307909.1:n.*331G=
NM_004915.4:c.*331G= NP_004906.3:n.*331G=
NM_016818.3:c.*331G= MANE Select NP_058198.2:n.*331G=
NM_207627.2:c.*331G= NP_997510.1:n.*331G=
NM_207629.2:c.*331G= NP_997512.1:n.*331G=