Canonical Allele Identifier: CA1181573549
Gene: ABCD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94418498A= , CM000663.2:g.94418498A= GRCh38
NC_000001.10:g.94884054A= , CM000663.1:g.94884054A= GRCh37
NC_000001.9:g.94656642A= NCBI36
NG_008865.1:g.5122A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370214.9:c.20A= MANE Select ENSP00000359233.4:p.Tyr7=
ENST00000647998.2:c.20A= ENSP00000497921.2:p.Tyr7=
ENST00000315713.5:c.20A= ENSP00000326880.5:p.Tyr7=
ENST00000370214.8:c.20A= ENSP00000359233.4:p.Tyr7=
NM_001122674.1:c.20A= NP_001116146.1:p.Tyr7=
NM_002858.3:c.20A= NP_002849.1:p.Tyr7=
XM_006710802.2:c.20A= XP_006710865.2:p.Tyr7=
NM_002858.4:c.20A= MANE Select NP_002849.1:p.Tyr7=
NM_001122674.2:c.20A= NP_001116146.1:p.Tyr7=