Canonical Allele Identifier: CA1004588932

Gene: ABCD3

Linked Data

• dbSNP Id: rs1659109437
• gnomAD v3: 1-94418442-C-CGCG
• gnomAD v4: 1-94418442-C-CGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94418443_94418445dup , CM000663.2:g.94418443_94418445dup	GRCh38
NC_000001.10:g.94883999_94884001dup , CM000663.1:g.94883999_94884001dup	GRCh37
NC_000001.9:g.94656587_94656589dup	NCBI36
NG_008865.1:g.5067_5069dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370214.9:c.-36_-34dup MANE Select	ENSP00000359233.4:n.-36_-34dup
NM_001122674.1:c.-36_-34dup	NP_001116146.1:n.-36_-34dup
NM_002858.3:c.-36_-34dup	NP_002849.1:n.-36_-34dup
XM_006710802.2:c.-36_-34dup	XP_006710865.2:n.-36_-34dup
NM_002858.4:c.-36_-34dup MANE Select	NP_002849.1:n.-36_-34dup
NM_001122674.2:c.-36_-34dup	NP_001116146.1:n.-36_-34dup