Canonical Allele Identifier: CA2176303607
Gene: SLC27A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50217432A= , CM000677.2:g.50217432A= GRCh38
NC_000015.9:g.50509629A= , CM000677.1:g.50509629A= GRCh37
NC_000015.8:g.48296921A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000267842.10:c.973-5533A= MANE Select ENSP00000267842.5:n.973-5533A=
ENST00000267842.9:c.973-5533A= ENSP00000267842.5:n.973-5533A=
ENST00000380902.8:c.814-5533A= ENSP00000370289.4:n.814-5533A=
ENST00000544960.1:c.268-5533A= ENSP00000444549.1:n.268-5533A=
ENST00000559938.1:n.12-5533A=
NM_001159629.1:c.814-5533A= NP_001153101.1:n.814-5533A=
NM_003645.3:c.973-5533A= NP_003636.2:n.973-5533A=
NM_003645.4:c.973-5533A= MANE Select NP_003636.2:n.973-5533A=
NM_001159629.2:c.814-5533A= NP_001153101.1:n.814-5533A=
Search 100 bp 5'
Search 100 bp 3'