Canonical Allele Identifier: CA713512815
Gene: SLC27A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50217394C>G , CM000677.2:g.50217394C>G GRCh38
NC_000015.9:g.50509591C>G , CM000677.1:g.50509591C>G GRCh37
NC_000015.8:g.48296883C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000267842.10:c.973-5571C>G MANE Select ENSP00000267842.5:n.973-5571C>G
ENST00000267842.9:c.973-5571C>G ENSP00000267842.5:n.973-5571C>G
ENST00000380902.8:c.814-5571C>G ENSP00000370289.4:n.814-5571C>G
ENST00000544960.1:c.268-5571C>G ENSP00000444549.1:n.268-5571C>G
ENST00000559938.1:n.12-5571C>G
NM_001159629.1:c.814-5571C>G NP_001153101.1:n.814-5571C>G
NM_003645.3:c.973-5571C>G NP_003636.2:n.973-5571C>G
NM_003645.4:c.973-5571C>G MANE Select NP_003636.2:n.973-5571C>G
NM_001159629.2:c.814-5571C>G NP_001153101.1:n.814-5571C>G
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