Canonical Allele Identifier: CA2390736099
Gene: ABCG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42296694T= , CM000683.2:g.42296694T= GRCh38
NC_000021.8:g.43716804T= , CM000683.1:g.43716804T= GRCh37
NC_000021.7:g.42589873T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398449.8:c.*302T= MANE Select ENSP00000381467.3:n.*302T=
ENST00000343687.7:c.*302T= ENSP00000339744.3:n.*302T=
ENST00000347800.6:c.*302T= ENSP00000291524.4:n.*302T=
ENST00000361802.6:c.*302T= ENSP00000354995.2:n.*302T=
ENST00000398437.1:c.*302T= ENSP00000381464.1:n.*302T=
ENST00000398449.7:c.*302T= ENSP00000381467.3:n.*302T=
ENST00000398457.6:c.*302T= ENSP00000381475.2:n.*302T=
ENST00000462050.5:n.2487T=
ENST00000472587.5:n.2353T=
NM_004915.3:c.*302T= NP_004906.3:n.*302T=
NM_016818.2:c.*302T= NP_058198.2:n.*302T=
NM_207174.1:c.*302T= NP_997057.1:n.*302T=
NM_207627.1:c.*302T= NP_997510.1:n.*302T=
NM_207628.1:c.*302T= NP_997511.1:n.*302T=
NM_207629.1:c.*302T= NP_997512.1:n.*302T=
XM_011529806.1:c.*302T= XP_011528108.1:n.*302T=
XM_011529807.1:c.*468T= XP_011528109.1:n.*468T=
XM_011529807.3:c.*468T= XP_011528109.1:n.*468T=
XM_024452141.1:c.*302T= XP_024307909.1:n.*302T=
NM_004915.4:c.*302T= NP_004906.3:n.*302T=
NM_016818.3:c.*302T= MANE Select NP_058198.2:n.*302T=
NM_207627.2:c.*302T= NP_997510.1:n.*302T=
NM_207629.2:c.*302T= NP_997512.1:n.*302T=