Canonical Allele Identifier: CA2644169992

Gene: LDLRAP1

Linked Data

• gnomAD v4: 1-25557283-T-TGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557287_25557288insGGGGG , CM000663.2:g.25557287_25557288insGGGGG	GRCh38
NC_000001.10:g.25883778_25883779insGGGGG , CM000663.1:g.25883778_25883779insGGGGG	GRCh37
NC_000001.9:g.25756365_25756366insGGGGG	NCBI36
NG_008932.1:g.18703_18704insGGGGG , LRG_276:g.18703_18704insGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.459+20_459+21insGGGGG MANE Select	ENSP00000363458.4:n.459+20_459+21insGGGGG
ENST00000374338.4:c.459+20_459+21insGGGGG	ENSP00000363458.4:n.459+20_459+21insGGGGG
ENST00000462394.1:n.227_228insGGGGG
ENST00000488127.1:n.929+20_929+21insGGGGG
NM_015627.2:c.459+20_459+21insGGGGG , LRG_276t1:c.459+20_459+21insGGGGG	NP_056442.2:n.459+20_459+21insGGGGG
XM_006710559.2:c.459+20_459+21insGGGGG	XP_006710622.1:n.459+20_459+21insGGGGG
XM_006710560.2:c.459+20_459+21insGGGGG	XP_006710623.1:n.459+20_459+21insGGGGG
XM_006710561.2:c.459+20_459+21insGGGGG	XP_006710624.1:n.459+20_459+21insGGGGG
XM_011541209.1:c.459+20_459+21insGGGGG	XP_011539511.1:n.459+20_459+21insGGGGG
XM_011541210.1:c.459+20_459+21insGGGGG	XP_011539512.1:n.459+20_459+21insGGGGG
XM_011541211.1:c.459+20_459+21insGGGGG	XP_011539513.1:n.459+20_459+21insGGGGG
XM_011541212.1:c.459+20_459+21insGGGGG	XP_011539514.1:n.459+20_459+21insGGGGG
XR_426598.2:n.578+20_578+21insGGGGG
XR_946602.1:n.578+20_578+21insGGGGG
XR_946603.1:n.578+20_578+21insGGGGG
XM_006710559.4:c.459+20_459+21insGGGGG	XP_006710622.1:n.459+20_459+21insGGGGG
XM_006710560.4:c.459+20_459+21insGGGGG	XP_006710623.1:n.459+20_459+21insGGGGG
XM_006710561.4:c.459+20_459+21insGGGGG	XP_006710624.1:n.459+20_459+21insGGGGG
XM_011541209.3:c.459+20_459+21insGGGGG	XP_011539511.1:n.459+20_459+21insGGGGG
XM_011541210.3:c.459+20_459+21insGGGGG	XP_011539512.1:n.459+20_459+21insGGGGG
XM_011541211.3:c.459+20_459+21insGGGGG	XP_011539513.1:n.459+20_459+21insGGGGG
XM_011541212.3:c.459+20_459+21insGGGGG	XP_011539514.1:n.459+20_459+21insGGGGG
XM_017000994.2:c.378+20_378+21insGGGGG	XP_016856483.1:n.378+20_378+21insGGGGG
XM_017000995.2:c.459+20_459+21insGGGGG	XP_016856484.1:n.459+20_459+21insGGGGG
XM_024446315.1:c.324+20_324+21insGGGGG	XP_024302083.1:n.324+20_324+21insGGGGG
XR_001737112.2:n.529+20_529+21insGGGGG
XR_001737113.2:n.529+20_529+21insGGGGG
XR_002956258.1:n.529+20_529+21insGGGGG
XR_426598.4:n.529+20_529+21insGGGGG
XR_946602.3:n.529+20_529+21insGGGGG
XR_946603.3:n.529+20_529+21insGGGGG
NM_015627.3:c.459+20_459+21insGGGGG MANE Select	NP_056442.2:n.459+20_459+21insGGGGG