Canonical Allele Identifier: CA1610232248
Gene: ELOVL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982278T= , CM000668.2:g.10982278T= GRCh38
NC_000006.11:g.10982511T= , CM000668.1:g.10982511T= GRCh37
NC_000006.10:g.11090497T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354666.4:c.*1503A= MANE Select ENSP00000346693.3:n.*1503A=
ENST00000354666.3:c.*1503A= ENSP00000346693.3:n.*1503A=
NM_017770.3:c.*1503A= NP_060240.3:n.*1503A=
XM_011514716.1:c.*1503A= XP_011513018.1:n.*1503A=
XM_011514717.1:c.*1503A= XP_011513019.1:n.*1503A=
XM_011514716.3:c.*1503A= XP_011513018.1:n.*1503A=
NM_017770.4:c.*1503A= MANE Select NP_060240.3:n.*1503A=
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