Canonical Allele Identifier: CA821639250

Gene: LPA

Linked Data

• dbSNP Id: rs1260436319
• MyVariant Identifiers: chr6:g.160962621_160962622insGATCCTGAG (hg19) ; chr6:g.160541589_160541590insGATCCTGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160541590_160541598dup , CM000668.2:g.160541590_160541598dup	GRCh38
NC_000006.11:g.160962622_160962630dup , CM000668.1:g.160962622_160962630dup	GRCh37
NC_000006.10:g.160882612_160882620dup	NCBI36
NG_016147.1:g.129778_129786dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.5520-417_5520-409dup MANE Select	ENSP00000321334.6:n.5520-417_5520-409dup
ENST00000316300.9:c.5520-417_5520-409dup	ENSP00000321334.5:n.5520-417_5520-409dup
NM_005577.2:c.5520-417_5520-409dup	NP_005568.2:n.5520-417_5520-409dup
NM_005577.3:c.5520-417_5520-409dup	NP_005568.2:n.5520-417_5520-409dup
NM_005577.4:c.5520-417_5520-409dup MANE Select	NP_005568.2:n.5520-417_5520-409dup