Canonical Allele Identifier: CA1140099885
Gene: LDLRAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25563141T= , CM000663.2:g.25563141T= GRCh38
NC_000001.10:g.25889632T= , CM000663.1:g.25889632T= GRCh37
NC_000001.9:g.25762219T= NCBI36
NG_008932.1:g.24557T= , LRG_276:g.24557T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374338.5:c.604T= MANE Select ENSP00000363458.4:p.Ser202=
ENST00000374338.4:c.604T= ENSP00000363458.4:p.Ser202=
ENST00000484476.5:n.326T=
ENST00000488127.1:n.1074T=
NM_015627.2:c.604T= , LRG_276t1:c.604T= NP_056442.2:p.Ser202=
XM_006710559.2:c.604T= XP_006710622.1:p.Ser202=
XM_006710560.2:c.604T= XP_006710623.1:p.Ser202=
XM_006710561.2:c.604T= XP_006710624.1:p.Ser202=
XM_011541209.1:c.604T= XP_011539511.1:p.Ser202=
XM_011541210.1:c.604T= XP_011539512.1:p.Ser202=
XM_011541211.1:c.604T= XP_011539513.1:p.Ser202=
XM_011541212.1:c.604T= XP_011539514.1:p.Ser202=
XR_426598.2:n.723T=
XR_946602.1:n.723T=
XR_946603.1:n.723T=
XM_006710559.4:c.604T= XP_006710622.1:p.Ser202=
XM_006710560.4:c.604T= XP_006710623.1:p.Ser202=
XM_006710561.4:c.604T= XP_006710624.1:p.Ser202=
XM_011541209.3:c.604T= XP_011539511.1:p.Ser202=
XM_011541210.3:c.604T= XP_011539512.1:p.Ser202=
XM_011541211.3:c.604T= XP_011539513.1:p.Ser202=
XM_011541212.3:c.604T= XP_011539514.1:p.Ser202=
XM_017000994.2:c.523T= XP_016856483.1:p.Ser175=
XM_017000995.2:c.459+5874T= XP_016856484.1:n.459+5874T=
XM_024446315.1:c.469T= XP_024302083.1:p.Ser157=
XR_001737112.2:n.674T=
XR_001737113.2:n.674T=
XR_002956258.1:n.674T=
XR_426598.4:n.674T=
XR_946602.3:n.674T=
XR_946603.3:n.674T=
NM_015627.3:c.604T= MANE Select NP_056442.2:p.Ser202=