Canonical Allele Identifier: CA2272580273
Gene: ABCA5 HGNC NCBI

Linked Data

dbSNP Id: rs2075045780

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69253906T>C , CM000679.2:g.69253906T>C GRCh38
NC_000017.10:g.67250047T>C , CM000679.1:g.67250047T>C GRCh37
NC_000017.9:g.64761642T>C NCBI36
NG_034199.1:g.78277A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392676.8:c.4245-37A>G MANE Select ENSP00000376443.2:n.4245-37A>G
ENST00000392676.7:c.4245-37A>G ENSP00000376443.2:n.4245-37A>G
ENST00000586811.1:c.1143-37A>G ENSP00000465351.1:n.1143-37A>G
ENST00000586995.5:c.3307-37A>G ENSP00000467251.1:n.3307-37A>G
ENST00000588877.5:c.4245-37A>G ENSP00000467882.1:n.4245-37A>G
ENST00000591234.5:c.2187-37A>G ENSP00000465766.1:n.2187-37A>G
NM_018672.4:c.4245-37A>G NP_061142.2:n.4245-37A>G
NM_172232.3:c.4245-37A>G NP_758424.1:n.4245-37A>G
NM_172232.4:c.4245-37A>G MANE Select NP_758424.1:n.4245-37A>G
NM_018672.5:c.4245-37A>G NP_061142.2:n.4245-37A>G