Canonical Allele Identifier: CA1146014504
Gene: ABCD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94418539C= , CM000663.2:g.94418539C= GRCh38
NC_000001.10:g.94884095C= , CM000663.1:g.94884095C= GRCh37
NC_000001.9:g.94656683C= NCBI36
NG_008865.1:g.5163C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370214.9:c.61C= MANE Select ENSP00000359233.4:p.Leu21=
ENST00000647998.2:c.61C= ENSP00000497921.2:p.Leu21=
ENST00000315713.5:c.61C= ENSP00000326880.5:p.Leu21=
ENST00000370214.8:c.61C= ENSP00000359233.4:p.Leu21=
NM_001122674.1:c.61C= NP_001116146.1:p.Leu21=
NM_002858.3:c.61C= NP_002849.1:p.Leu21=
XM_006710802.2:c.61C= XP_006710865.2:p.Leu21=
NM_002858.4:c.61C= MANE Select NP_002849.1:p.Leu21=
NM_001122674.2:c.61C= NP_001116146.1:p.Leu21=