Canonical Allele Identifier: CA2644170009

Gene: LDLRAP1

Linked Data

• gnomAD v4: 1-25557288-C-CGGGGGGGTGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557292_25557293insGGGTGGGGGGGGGGGGGG , CM000663.2:g.25557292_25557293insGGGTGGGGGGGGGGGGGG	GRCh38
NC_000001.10:g.25883783_25883784insGGGTGGGGGGGGGGGGGG , CM000663.1:g.25883783_25883784insGGGTGGGGGGGGGGGGGG	GRCh37
NC_000001.9:g.25756370_25756371insGGGTGGGGGGGGGGGGGG	NCBI36
NG_008932.1:g.18708_18709insGGGTGGGGGGGGGGGGGG , LRG_276:g.18708_18709insGGGTGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.459+25_459+26insGGGTGGGGGGGGGGGGGG MANE Select	ENSP00000363458.4:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
ENST00000374338.4:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	ENSP00000363458.4:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
ENST00000462394.1:n.232_233insGGGTGGGGGGGGGGGGGG
ENST00000488127.1:n.929+25_929+26insGGGTGGGGGGGGGGGGGG
NM_015627.2:c.459+25_459+26insGGGTGGGGGGGGGGGGGG , LRG_276t1:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	NP_056442.2:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_006710559.2:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_006710622.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_006710560.2:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_006710623.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_006710561.2:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_006710624.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541209.1:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539511.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541210.1:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539512.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541211.1:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539513.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541212.1:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539514.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XR_426598.2:n.578+25_578+26insGGGTGGGGGGGGGGGGGG
XR_946602.1:n.578+25_578+26insGGGTGGGGGGGGGGGGGG
XR_946603.1:n.578+25_578+26insGGGTGGGGGGGGGGGGGG
XM_006710559.4:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_006710622.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_006710560.4:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_006710623.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_006710561.4:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_006710624.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541209.3:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539511.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541210.3:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539512.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541211.3:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539513.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_011541212.3:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_011539514.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_017000994.2:c.378+25_378+26insGGGTGGGGGGGGGGGGGG	XP_016856483.1:n.378+25_378+26insGGGTGGGGGGGGGGGGGG
XM_017000995.2:c.459+25_459+26insGGGTGGGGGGGGGGGGGG	XP_016856484.1:n.459+25_459+26insGGGTGGGGGGGGGGGGGG
XM_024446315.1:c.324+25_324+26insGGGTGGGGGGGGGGGGGG	XP_024302083.1:n.324+25_324+26insGGGTGGGGGGGGGGGGGG
XR_001737112.2:n.529+25_529+26insGGGTGGGGGGGGGGGGGG
XR_001737113.2:n.529+25_529+26insGGGTGGGGGGGGGGGGGG
XR_002956258.1:n.529+25_529+26insGGGTGGGGGGGGGGGGGG
XR_426598.4:n.529+25_529+26insGGGTGGGGGGGGGGGGGG
XR_946602.3:n.529+25_529+26insGGGTGGGGGGGGGGGGGG
XR_946603.3:n.529+25_529+26insGGGTGGGGGGGGGGGGGG
NM_015627.3:c.459+25_459+26insGGGTGGGGGGGGGGGGGG MANE Select	NP_056442.2:n.459+25_459+26insGGGTGGGGGGGGGGGGGG