Canonical Allele Identifier: CA1610232192
Gene: ELOVL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982220_10982221delinsGA , CM000668.2:g.10982220_10982221delinsGA GRCh38
NC_000006.11:g.10982453_10982454delinsGA , CM000668.1:g.10982453_10982454delinsGA GRCh37
NC_000006.10:g.11090439_11090440delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354666.4:c.*1560_*1561delinsTC MANE Select ENSP00000346693.3:n.*1560_*1561delinsTC
ENST00000354666.3:c.*1560_*1561delinsTC ENSP00000346693.3:n.*1560_*1561delinsTC
NM_017770.3:c.*1560_*1561delinsTC NP_060240.3:n.*1560_*1561delinsTC
XM_011514716.1:c.*1560_*1561delinsTC XP_011513018.1:n.*1560_*1561delinsTC
XM_011514717.1:c.*1560_*1561delinsTC XP_011513019.1:n.*1560_*1561delinsTC
XM_011514716.3:c.*1560_*1561delinsTC XP_011513018.1:n.*1560_*1561delinsTC
NM_017770.4:c.*1560_*1561delinsTC MANE Select NP_060240.3:n.*1560_*1561delinsTC