Canonical Allele Identifier: CA1769106822
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957721_19957725delinsTCTGA , CM000670.2:g.19957721_19957725delinsTCTGA GRCh38
NC_000008.10:g.19815232_19815236delinsTCTGA , CM000670.1:g.19815232_19815236delinsTCTGA GRCh37
NC_000008.9:g.19859512_19859516delinsTCTGA NCBI36
NG_008855.1:g.23651_23655delinsTCTGA
NG_008855.2:g.61005_61009delinsTCTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-1539_1019-1535delinsTCTGA MANE Select ENSP00000497642.1:n.1019-1539_1019-1535de...
ENST00000650478.1:c.79+1638_79+1642delinsTCTGA ENSP00000497560.1:n.79+1638_79+1642delins...
ENST00000311322.8:c.1019-1539_1019-1535delinsTCTGA ENSP00000309757.6:n.1019-1539_1019-1535de...
NM_000237.2:c.1019-1539_1019-1535delinsTCTGA NP_000228.1:n.1019-1539_1019-1535delinsTC...
NM_000237.3:c.1019-1539_1019-1535delinsTCTGA MANE Select NP_000228.1:n.1019-1539_1019-1535delinsTC...