Canonical Allele Identifier: CA19669426

Gene: LDLRAP1

Linked Data

• ClinVar Variation Id: 2441156
• ClinVar RCV Id: RCV003146985
• dbSNP Id: rs1019504966
• gnomAD v2: 1-25870190-A-G
• gnomAD v3: 1-25543699-A-G
• gnomAD v4: 1-25543699-A-G
• MyVariant Identifiers: chr1:g.25870190A>G (hg19) ; chr1:g.25543699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25543699A>G , CM000663.2:g.25543699A>G	GRCh38
NC_000001.10:g.25870190A>G , CM000663.1:g.25870190A>G	GRCh37
NC_000001.9:g.25742777A>G	NCBI36
NG_008932.1:g.5115A>G , LRG_276:g.5115A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.1A>G MANE Select	ENSP00000363458.4:p.Met1Val
ENST00000374338.4:c.1A>G	ENSP00000363458.4:p.Met1Val
NM_015627.2:c.1A>G , LRG_276t1:c.1A>G	NP_056442.2:p.Met1Val
XM_006710559.2:c.1A>G	XP_006710622.1:p.Met1Val
XM_006710560.2:c.1A>G	XP_006710623.1:p.Met1Val
XM_006710561.2:c.1A>G	XP_006710624.1:p.Met1Val
XM_011541209.1:c.1A>G	XP_011539511.1:p.Met1Val
XM_011541210.1:c.1A>G	XP_011539512.1:p.Met1Val
XM_011541211.1:c.1A>G	XP_011539513.1:p.Met1Val
XM_011541212.1:c.1A>G	XP_011539514.1:p.Met1Val
XR_426598.2:n.120A>G
XR_946602.1:n.120A>G
XR_946603.1:n.120A>G
XM_006710559.4:c.1A>G	XP_006710622.1:p.Met1Val
XM_006710560.4:c.1A>G	XP_006710623.1:p.Met1Val
XM_006710561.4:c.1A>G	XP_006710624.1:p.Met1Val
XM_011541209.3:c.1A>G	XP_011539511.1:p.Met1Val
XM_011541210.3:c.1A>G	XP_011539512.1:p.Met1Val
XM_011541211.3:c.1A>G	XP_011539513.1:p.Met1Val
XM_011541212.3:c.1A>G	XP_011539514.1:p.Met1Val
XM_017000995.2:c.1A>G	XP_016856484.1:p.Met1Val
XR_001737112.2:n.71A>G
XR_001737113.2:n.71A>G
XR_002956258.1:n.71A>G
XR_426598.4:n.71A>G
XR_946602.3:n.71A>G
XR_946603.3:n.71A>G
NM_015627.3:c.1A>G MANE Select	NP_056442.2:p.Met1Val