Canonical Allele Identifier: CA2176303689
Gene: SLC27A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50217500G= , CM000677.2:g.50217500G= GRCh38
NC_000015.9:g.50509697G= , CM000677.1:g.50509697G= GRCh37
NC_000015.8:g.48296989G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000267842.10:c.973-5465G= MANE Select ENSP00000267842.5:n.973-5465G=
ENST00000267842.9:c.973-5465G= ENSP00000267842.5:n.973-5465G=
ENST00000380902.8:c.814-5465G= ENSP00000370289.4:n.814-5465G=
ENST00000544960.1:c.268-5465G= ENSP00000444549.1:n.268-5465G=
ENST00000559938.1:n.12-5465G=
NM_001159629.1:c.814-5465G= NP_001153101.1:n.814-5465G=
NM_003645.3:c.973-5465G= NP_003636.2:n.973-5465G=
NM_003645.4:c.973-5465G= MANE Select NP_003636.2:n.973-5465G=
NM_001159629.2:c.814-5465G= NP_001153101.1:n.814-5465G=
Search 100 bp 5'
Search 100 bp 3'