Canonical Allele Identifier: CA415111874
Community Standard Title: NM_000033.4(ABCD1):c.1611G>T (p.Gln537His)
Gene: ABCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153740214G>T , CM000685.2:g.153740214G>T GRCh38
NC_000023.10:g.153005668G>T , CM000685.1:g.153005668G>T GRCh37
NC_000023.9:g.152658862G>T NCBI36
NG_009022.2:g.20347G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000033.4:c.1611G>T MANE Select NP_000024.2:p.Gln537His
ENST00000218104.6:c.1611G>T MANE Select ENSP00000218104.3:p.Gln537His
NM_000033.3:c.1611G>T NP_000024.2:p.Gln537His
ENST00000218104.5:c.1611G>T ENSP00000218104.3:p.Gln537His
ENST00000443684.2:n.614G>T
XR_938507.1:n.2083G>T
XR_938507.2:n.2083G>T