Canonical Allele Identifier: CA339078766
Gene: LDLRAP1 HGNC NCBI

Linked Data

dbSNP Id: rs2044225261

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25557246C>G , CM000663.2:g.25557246C>G GRCh38
NC_000001.10:g.25883737C>G , CM000663.1:g.25883737C>G GRCh37
NC_000001.9:g.25756324C>G NCBI36
NG_008932.1:g.18662C>G , LRG_276:g.18662C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.438C>G MANE Select ENSP00000363458.4:p.Phe146Leu
ENST00000374338.4:c.438C>G ENSP00000363458.4:p.Phe146Leu
ENST00000462394.1:n.186C>G
ENST00000488127.1:n.908C>G
NM_015627.2:c.438C>G , LRG_276t1:c.438C>G NP_056442.2:p.Phe146Leu
XM_006710559.2:c.438C>G XP_006710622.1:p.Phe146Leu
XM_006710560.2:c.438C>G XP_006710623.1:p.Phe146Leu
XM_006710561.2:c.438C>G XP_006710624.1:p.Phe146Leu
XM_011541209.1:c.438C>G XP_011539511.1:p.Phe146Leu
XM_011541210.1:c.438C>G XP_011539512.1:p.Phe146Leu
XM_011541211.1:c.438C>G XP_011539513.1:p.Phe146Leu
XM_011541212.1:c.438C>G XP_011539514.1:p.Phe146Leu
XR_426598.2:n.557C>G
XR_946602.1:n.557C>G
XR_946603.1:n.557C>G
XM_006710559.4:c.438C>G XP_006710622.1:p.Phe146Leu
XM_006710560.4:c.438C>G XP_006710623.1:p.Phe146Leu
XM_006710561.4:c.438C>G XP_006710624.1:p.Phe146Leu
XM_011541209.3:c.438C>G XP_011539511.1:p.Phe146Leu
XM_011541210.3:c.438C>G XP_011539512.1:p.Phe146Leu
XM_011541211.3:c.438C>G XP_011539513.1:p.Phe146Leu
XM_011541212.3:c.438C>G XP_011539514.1:p.Phe146Leu
XM_017000994.2:c.357C>G XP_016856483.1:p.Phe119Leu
XM_017000995.2:c.438C>G XP_016856484.1:p.Phe146Leu
XM_024446315.1:c.303C>G XP_024302083.1:p.Phe101Leu
XR_001737112.2:n.508C>G
XR_001737113.2:n.508C>G
XR_002956258.1:n.508C>G
XR_426598.4:n.508C>G
XR_946602.3:n.508C>G
XR_946603.3:n.508C>G
NM_015627.3:c.438C>G MANE Select NP_056442.2:p.Phe146Leu