Canonical Allele Identifier: CA10609975

Gene: LDLRAP1

Linked Data

• ClinVar Variation Id: 296966
• ClinVar RCV Id: RCV000295278
• dbSNP Id: rs575569789
• gnomAD v2: 1-25870098-G-T
• gnomAD v3: 1-25543607-G-T
• gnomAD v4: 1-25543607-G-T
• MyVariant Identifiers: chr1:g.25870098G>T (hg19) ; chr1:g.25543607G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25543607G>T , CM000663.2:g.25543607G>T	GRCh38
NC_000001.10:g.25870098G>T , CM000663.1:g.25870098G>T	GRCh37
NC_000001.9:g.25742685G>T	NCBI36
NG_008932.1:g.5023G>T , LRG_276:g.5023G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374338.5:c.-92G>T MANE Select	ENSP00000363458.4:n.-92G>T
ENST00000374338.4:c.-92G>T	ENSP00000363458.4:n.-92G>T
NM_015627.2:c.-92G>T , LRG_276t1:c.-92G>T	NP_056442.2:n.-92G>T
XM_006710559.2:c.-92G>T	XP_006710622.1:n.-92G>T
XM_006710560.2:c.-92G>T	XP_006710623.1:n.-92G>T
XM_006710561.2:c.-92G>T	XP_006710624.1:n.-92G>T
XM_011541209.1:c.-92G>T	XP_011539511.1:n.-92G>T
XM_011541210.1:c.-92G>T	XP_011539512.1:n.-92G>T
XM_011541211.1:c.-92G>T	XP_011539513.1:n.-92G>T
XM_011541212.1:c.-92G>T	XP_011539514.1:n.-92G>T
XR_426598.2:n.28G>T
XR_946602.1:n.28G>T
XR_946603.1:n.28G>T
XM_017000995.2:c.-92G>T	XP_016856484.1:n.-92G>T
NM_015627.3:c.-92G>T MANE Select	NP_056442.2:n.-92G>T