Canonical Allele Identifier: CA1159704281

Gene: LDLRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557328_25557329delinsTG , CM000663.2:g.25557328_25557329delinsTG	GRCh38
NC_000001.10:g.25883819_25883820delinsTG , CM000663.1:g.25883819_25883820delinsTG	GRCh37
NC_000001.9:g.25756406_25756407delinsTG	NCBI36
NG_008932.1:g.18744_18745delinsTG , LRG_276:g.18744_18745delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.459+61_459+62delinsTG MANE Select	ENSP00000363458.4:n.459+61_459+62delinsTG
ENST00000374338.4:c.459+61_459+62delinsTG	ENSP00000363458.4:n.459+61_459+62delinsTG
ENST00000462394.1:n.268_269delinsTG
ENST00000488127.1:n.929+61_929+62delinsTG
NM_015627.2:c.459+61_459+62delinsTG , LRG_276t1:c.459+61_459+62delinsTG	NP_056442.2:n.459+61_459+62delinsTG
XM_006710559.2:c.459+61_459+62delinsTG	XP_006710622.1:n.459+61_459+62delinsTG
XM_006710560.2:c.459+61_459+62delinsTG	XP_006710623.1:n.459+61_459+62delinsTG
XM_006710561.2:c.459+61_459+62delinsTG	XP_006710624.1:n.459+61_459+62delinsTG
XM_011541209.1:c.459+61_459+62delinsTG	XP_011539511.1:n.459+61_459+62delinsTG
XM_011541210.1:c.459+61_459+62delinsTG	XP_011539512.1:n.459+61_459+62delinsTG
XM_011541211.1:c.459+61_459+62delinsTG	XP_011539513.1:n.459+61_459+62delinsTG
XM_011541212.1:c.459+61_459+62delinsTG	XP_011539514.1:n.459+61_459+62delinsTG
XR_426598.2:n.578+61_578+62delinsTG
XR_946602.1:n.578+61_578+62delinsTG
XR_946603.1:n.578+61_578+62delinsTG
XM_006710559.4:c.459+61_459+62delinsTG	XP_006710622.1:n.459+61_459+62delinsTG
XM_006710560.4:c.459+61_459+62delinsTG	XP_006710623.1:n.459+61_459+62delinsTG
XM_006710561.4:c.459+61_459+62delinsTG	XP_006710624.1:n.459+61_459+62delinsTG
XM_011541209.3:c.459+61_459+62delinsTG	XP_011539511.1:n.459+61_459+62delinsTG
XM_011541210.3:c.459+61_459+62delinsTG	XP_011539512.1:n.459+61_459+62delinsTG
XM_011541211.3:c.459+61_459+62delinsTG	XP_011539513.1:n.459+61_459+62delinsTG
XM_011541212.3:c.459+61_459+62delinsTG	XP_011539514.1:n.459+61_459+62delinsTG
XM_017000994.2:c.378+61_378+62delinsTG	XP_016856483.1:n.378+61_378+62delinsTG
XM_017000995.2:c.459+61_459+62delinsTG	XP_016856484.1:n.459+61_459+62delinsTG
XM_024446315.1:c.324+61_324+62delinsTG	XP_024302083.1:n.324+61_324+62delinsTG
XR_001737112.2:n.529+61_529+62delinsTG
XR_001737113.2:n.529+61_529+62delinsTG
XR_002956258.1:n.529+61_529+62delinsTG
XR_426598.4:n.529+61_529+62delinsTG
XR_946602.3:n.529+61_529+62delinsTG
XR_946603.3:n.529+61_529+62delinsTG
NM_015627.3:c.459+61_459+62delinsTG MANE Select	NP_056442.2:n.459+61_459+62delinsTG