Canonical Allele Identifier: CA339078812

Gene: LDLRAP1

Linked Data

• dbSNP Id: rs1278158715
• gnomAD v2: 1-25883758-G-A
• gnomAD v4: 1-25557267-G-A
• MyVariant Identifiers: chr1:g.25883758G>A (hg19) ; chr1:g.25557267G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557267G>A , CM000663.2:g.25557267G>A	GRCh38
NC_000001.10:g.25883758G>A , CM000663.1:g.25883758G>A	GRCh37
NC_000001.9:g.25756345G>A	NCBI36
NG_008932.1:g.18683G>A , LRG_276:g.18683G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.459G>A MANE Select	ENSP00000363458.4:p.Met153Ile
ENST00000374338.4:c.459G>A	ENSP00000363458.4:p.Met153Ile
ENST00000462394.1:n.207G>A
ENST00000488127.1:n.929G>A
NM_015627.2:c.459G>A , LRG_276t1:c.459G>A	NP_056442.2:p.Met153Ile
XM_006710559.2:c.459G>A	XP_006710622.1:p.Met153Ile
XM_006710560.2:c.459G>A	XP_006710623.1:p.Met153Ile
XM_006710561.2:c.459G>A	XP_006710624.1:p.Met153Ile
XM_011541209.1:c.459G>A	XP_011539511.1:p.Met153Ile
XM_011541210.1:c.459G>A	XP_011539512.1:p.Met153Ile
XM_011541211.1:c.459G>A	XP_011539513.1:p.Met153Ile
XM_011541212.1:c.459G>A	XP_011539514.1:p.Met153Ile
XR_426598.2:n.578G>A
XR_946602.1:n.578G>A
XR_946603.1:n.578G>A
XM_006710559.4:c.459G>A	XP_006710622.1:p.Met153Ile
XM_006710560.4:c.459G>A	XP_006710623.1:p.Met153Ile
XM_006710561.4:c.459G>A	XP_006710624.1:p.Met153Ile
XM_011541209.3:c.459G>A	XP_011539511.1:p.Met153Ile
XM_011541210.3:c.459G>A	XP_011539512.1:p.Met153Ile
XM_011541211.3:c.459G>A	XP_011539513.1:p.Met153Ile
XM_011541212.3:c.459G>A	XP_011539514.1:p.Met153Ile
XM_017000994.2:c.378G>A	XP_016856483.1:p.Met126Ile
XM_017000995.2:c.459G>A	XP_016856484.1:p.Met153Ile
XM_024446315.1:c.324G>A	XP_024302083.1:p.Met108Ile
XR_001737112.2:n.529G>A
XR_001737113.2:n.529G>A
XR_002956258.1:n.529G>A
XR_426598.4:n.529G>A
XR_946602.3:n.529G>A
XR_946603.3:n.529G>A
NM_015627.3:c.459G>A MANE Select	NP_056442.2:p.Met153Ile