Canonical Allele Identifier: CA370469375
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19956042-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956042G>C , CM000670.2:g.19956042G>C GRCh38
NC_000008.10:g.19813553G>C , CM000670.1:g.19813553G>C GRCh37
NC_000008.9:g.19857833G>C NCBI36
NG_008855.1:g.21972G>C
NG_008855.2:g.59326G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.977G>C MANE Select ENSP00000497642.1:p.Ser326Thr
ENST00000650478.1:c.38G>C ENSP00000497560.1:p.Ser13Thr
ENST00000311322.8:c.977G>C ENSP00000309757.6:p.Ser326Thr
NM_000237.2:c.977G>C NP_000228.1:p.Ser326Thr
NM_000237.3:c.977G>C MANE Select NP_000228.1:p.Ser326Thr