Canonical Allele Identifier: CA1159706437

Gene: LDLRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25566928C= , CM000663.2:g.25566928C=	GRCh38
NC_000001.10:g.25893419C= , CM000663.1:g.25893419C=	GRCh37
NC_000001.9:g.25766006C=	NCBI36
NG_008932.1:g.28344C= , LRG_276:g.28344C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015627.3:c.863C= MANE Select	NP_056442.2:p.Ser288=
ENST00000374338.5:c.863C= MANE Select	ENSP00000363458.4:p.Ser288=
NM_015627.2:c.863C= , LRG_276t1:c.863C=	NP_056442.2:p.Ser288=
ENST00000374338.4:c.863C=	ENSP00000363458.4:p.Ser288=
ENST00000470950.1:n.287C=
ENST00000474283.1:n.271C=
ENST00000484476.5:n.585C=
ENST00000488127.1:n.2714C=
XM_006710559.4:c.*1512C=	XP_006710622.1:n.*1512C=
XM_006710560.2:c.782+1721C=	XP_006710623.1:n.782+1721C=
XM_006710560.4:c.782+1721C=	XP_006710623.1:n.782+1721C=
XM_006710561.2:c.782+1721C=	XP_006710624.1:n.782+1721C=
XM_006710561.4:c.782+1721C=	XP_006710624.1:n.782+1721C=
XM_011541209.1:c.860C=	XP_011539511.1:p.Ser287=
XM_011541209.3:c.860C=	XP_011539511.1:p.Ser287=
XM_011541210.3:c.*1512C=	XP_011539512.1:n.*1512C=
XM_011541211.1:c.779+1721C=	XP_011539513.1:n.779+1721C=
XM_011541211.3:c.779+1721C=	XP_011539513.1:n.779+1721C=
XM_011541212.1:c.779+1721C=	XP_011539514.1:n.779+1721C=
XM_011541212.3:c.779+1721C=	XP_011539514.1:n.779+1721C=
XM_017000994.2:c.782C=	XP_016856483.1:p.Ser261=
XM_017000995.2:c.459+9661C=	XP_016856484.1:n.459+9661C=
XM_024446315.1:c.728C=	XP_024302083.1:p.Ser243=
XR_001737112.2:n.852+1721C=
XR_001737113.2:n.1043C=
XR_002956258.1:n.1903C=
XR_426598.4:n.1046C=
XR_946602.1:n.901+1721C=
XR_946602.3:n.852+1721C=
XR_946603.3:n.2331C=