Canonical Allele Identifier: CA339076572
Gene: LDLRAP1 HGNC NCBI

Linked Data

dbSNP Id: rs2043857912
gnomAD v4: 1-25543736-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25543736G>T , CM000663.2:g.25543736G>T GRCh38
NC_000001.10:g.25870227G>T , CM000663.1:g.25870227G>T GRCh37
NC_000001.9:g.25742814G>T NCBI36
NG_008932.1:g.5152G>T , LRG_276:g.5152G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.38G>T MANE Select ENSP00000363458.4:p.Arg13Leu
ENST00000374338.4:c.38G>T ENSP00000363458.4:p.Arg13Leu
NM_015627.2:c.38G>T , LRG_276t1:c.38G>T NP_056442.2:p.Arg13Leu
XM_006710559.2:c.38G>T XP_006710622.1:p.Arg13Leu
XM_006710560.2:c.38G>T XP_006710623.1:p.Arg13Leu
XM_006710561.2:c.38G>T XP_006710624.1:p.Arg13Leu
XM_011541209.1:c.38G>T XP_011539511.1:p.Arg13Leu
XM_011541210.1:c.38G>T XP_011539512.1:p.Arg13Leu
XM_011541211.1:c.38G>T XP_011539513.1:p.Arg13Leu
XM_011541212.1:c.38G>T XP_011539514.1:p.Arg13Leu
XR_426598.2:n.157G>T
XR_946602.1:n.157G>T
XR_946603.1:n.157G>T
XM_006710559.4:c.38G>T XP_006710622.1:p.Arg13Leu
XM_006710560.4:c.38G>T XP_006710623.1:p.Arg13Leu
XM_006710561.4:c.38G>T XP_006710624.1:p.Arg13Leu
XM_011541209.3:c.38G>T XP_011539511.1:p.Arg13Leu
XM_011541210.3:c.38G>T XP_011539512.1:p.Arg13Leu
XM_011541211.3:c.38G>T XP_011539513.1:p.Arg13Leu
XM_011541212.3:c.38G>T XP_011539514.1:p.Arg13Leu
XM_017000995.2:c.38G>T XP_016856484.1:p.Arg13Leu
XR_001737112.2:n.108G>T
XR_001737113.2:n.108G>T
XR_002956258.1:n.108G>T
XR_426598.4:n.108G>T
XR_946602.3:n.108G>T
XR_946603.3:n.108G>T
NM_015627.3:c.38G>T MANE Select NP_056442.2:p.Arg13Leu