Canonical Allele Identifier: CA339076398

Gene: LDLRAP1

Linked Data

• dbSNP Id: rs1049626491
• gnomAD v2: 1-25870164-AGCG-A
• gnomAD v3: 1-25543673-AGCG-A
• gnomAD v4: 1-25543673-AGCG-A
• MyVariant Identifiers: chr1:g.25870165_25870167del (hg19) ; chr1:g.25543675_25543677del (hg38) ; chr1:g.25543674_25543676del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25543685_25543687del , CM000663.2:g.25543685_25543687del	GRCh38
NC_000001.10:g.25870176_25870178del , CM000663.1:g.25870176_25870178del	GRCh37
NC_000001.9:g.25742763_25742765del	NCBI36
NG_008932.1:g.5101_5103del , LRG_276:g.5101_5103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.-14_-12del MANE Select	ENSP00000363458.4:n.-14_-12del
ENST00000374338.4:c.-14_-12del	ENSP00000363458.4:n.-14_-12del
NM_015627.2:c.-14_-12del , LRG_276t1:c.-14_-12del	NP_056442.2:n.-14_-12del
XM_006710559.2:c.-14_-12del	XP_006710622.1:n.-14_-12del
XM_006710560.2:c.-14_-12del	XP_006710623.1:n.-14_-12del
XM_006710561.2:c.-14_-12del	XP_006710624.1:n.-14_-12del
XM_011541209.1:c.-14_-12del	XP_011539511.1:n.-14_-12del
XM_011541210.1:c.-14_-12del	XP_011539512.1:n.-14_-12del
XM_011541211.1:c.-14_-12del	XP_011539513.1:n.-14_-12del
XM_011541212.1:c.-14_-12del	XP_011539514.1:n.-14_-12del
XR_426598.2:n.106_108del
XR_946602.1:n.106_108del
XR_946603.1:n.106_108del
XM_006710559.4:c.-14_-12del	XP_006710622.1:n.-14_-12del
XM_006710560.4:c.-14_-12del	XP_006710623.1:n.-14_-12del
XM_006710561.4:c.-14_-12del	XP_006710624.1:n.-14_-12del
XM_011541209.3:c.-14_-12del	XP_011539511.1:n.-14_-12del
XM_011541210.3:c.-14_-12del	XP_011539512.1:n.-14_-12del
XM_011541211.3:c.-14_-12del	XP_011539513.1:n.-14_-12del
XM_011541212.3:c.-14_-12del	XP_011539514.1:n.-14_-12del
XM_017000995.2:c.-14_-12del	XP_016856484.1:n.-14_-12del
XR_001737112.2:n.57_59del
XR_001737113.2:n.57_59del
XR_002956258.1:n.57_59del
XR_426598.4:n.57_59del
XR_946602.3:n.57_59del
XR_946603.3:n.57_59del
NM_015627.3:c.-14_-12del MANE Select	NP_056442.2:n.-14_-12del