Canonical Allele Identifier: CA571544605

Gene: LPA

Linked Data

• dbSNP Id: rs1273919371
• gnomAD v2: 6-160974534-T-A
• gnomAD v3: 6-160553502-T-A
• gnomAD v4: 6-160553502-T-A
• MyVariant Identifiers: chr6:g.160974534T>A (hg19) ; chr6:g.160553502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160553502T>A , CM000668.2:g.160553502T>A	GRCh38
NC_000006.11:g.160974534T>A , CM000668.1:g.160974534T>A	GRCh37
NC_000006.10:g.160894524T>A	NCBI36
NG_016147.1:g.117874A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.4973+2523A>T MANE Select	ENSP00000321334.6:n.4973+2523A>T
ENST00000316300.9:c.4973+2523A>T	ENSP00000321334.5:n.4973+2523A>T
NM_005577.2:c.4973+2523A>T	NP_005568.2:n.4973+2523A>T
NM_005577.3:c.4973+2523A>T	NP_005568.2:n.4973+2523A>T
NM_005577.4:c.4973+2523A>T MANE Select	NP_005568.2:n.4973+2523A>T