Canonical Allele Identifier: CA521716268

Gene: LDLRAP1

Linked Data

• dbSNP Id: rs1394276020
• gnomAD v2: 1-25883898-A-ATTGG
• gnomAD v3: 1-25557407-A-ATTGG
• gnomAD v4: 1-25557407-A-ATTGG
• MyVariant Identifiers: chr1:g.25883898_25883899insTTGG (hg19) ; chr1:g.25557407_25557408insTTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557407_25557408insTTGG , CM000663.2:g.25557407_25557408insTTGG	GRCh38
NC_000001.10:g.25883898_25883899insTTGG , CM000663.1:g.25883898_25883899insTTGG	GRCh37
NC_000001.9:g.25756485_25756486insTTGG	NCBI36
NG_008932.1:g.18823_18824insTTGG , LRG_276:g.18823_18824insTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.459+140_459+141insTTGG MANE Select	ENSP00000363458.4:n.459+140_459+141insTTGG
ENST00000374338.4:c.459+140_459+141insTTGG	ENSP00000363458.4:n.459+140_459+141insTTGG
ENST00000462394.1:n.347_348insTTGG
ENST00000488127.1:n.929+140_929+141insTTGG
NM_015627.2:c.459+140_459+141insTTGG , LRG_276t1:c.459+140_459+141insTTGG	NP_056442.2:n.459+140_459+141insTTGG
XM_006710559.2:c.459+140_459+141insTTGG	XP_006710622.1:n.459+140_459+141insTTGG
XM_006710560.2:c.459+140_459+141insTTGG	XP_006710623.1:n.459+140_459+141insTTGG
XM_006710561.2:c.459+140_459+141insTTGG	XP_006710624.1:n.459+140_459+141insTTGG
XM_011541209.1:c.459+140_459+141insTTGG	XP_011539511.1:n.459+140_459+141insTTGG
XM_011541210.1:c.459+140_459+141insTTGG	XP_011539512.1:n.459+140_459+141insTTGG
XM_011541211.1:c.459+140_459+141insTTGG	XP_011539513.1:n.459+140_459+141insTTGG
XM_011541212.1:c.459+140_459+141insTTGG	XP_011539514.1:n.459+140_459+141insTTGG
XR_426598.2:n.578+140_578+141insTTGG
XR_946602.1:n.578+140_578+141insTTGG
XR_946603.1:n.578+140_578+141insTTGG
XM_006710559.4:c.459+140_459+141insTTGG	XP_006710622.1:n.459+140_459+141insTTGG
XM_006710560.4:c.459+140_459+141insTTGG	XP_006710623.1:n.459+140_459+141insTTGG
XM_006710561.4:c.459+140_459+141insTTGG	XP_006710624.1:n.459+140_459+141insTTGG
XM_011541209.3:c.459+140_459+141insTTGG	XP_011539511.1:n.459+140_459+141insTTGG
XM_011541210.3:c.459+140_459+141insTTGG	XP_011539512.1:n.459+140_459+141insTTGG
XM_011541211.3:c.459+140_459+141insTTGG	XP_011539513.1:n.459+140_459+141insTTGG
XM_011541212.3:c.459+140_459+141insTTGG	XP_011539514.1:n.459+140_459+141insTTGG
XM_017000994.2:c.378+140_378+141insTTGG	XP_016856483.1:n.378+140_378+141insTTGG
XM_017000995.2:c.459+140_459+141insTTGG	XP_016856484.1:n.459+140_459+141insTTGG
XM_024446315.1:c.324+140_324+141insTTGG	XP_024302083.1:n.324+140_324+141insTTGG
XR_001737112.2:n.529+140_529+141insTTGG
XR_001737113.2:n.529+140_529+141insTTGG
XR_002956258.1:n.529+140_529+141insTTGG
XR_426598.4:n.529+140_529+141insTTGG
XR_946602.3:n.529+140_529+141insTTGG
XR_946603.3:n.529+140_529+141insTTGG
NM_015627.3:c.459+140_459+141insTTGG MANE Select	NP_056442.2:n.459+140_459+141insTTGG