Canonical Allele Identifier: CA1159704008

Gene: LDLRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557222C= , CM000663.2:g.25557222C=	GRCh38
NC_000001.10:g.25883713C= , CM000663.1:g.25883713C=	GRCh37
NC_000001.9:g.25756300C=	NCBI36
NG_008932.1:g.18638C= , LRG_276:g.18638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.414C= MANE Select	ENSP00000363458.4:p.Asn138=
ENST00000374338.4:c.414C=	ENSP00000363458.4:p.Asn138=
ENST00000462394.1:n.162C=
ENST00000488127.1:n.884C=
NM_015627.2:c.414C= , LRG_276t1:c.414C=	NP_056442.2:p.Asn138=
XM_006710559.2:c.414C=	XP_006710622.1:p.Asn138=
XM_006710560.2:c.414C=	XP_006710623.1:p.Asn138=
XM_006710561.2:c.414C=	XP_006710624.1:p.Asn138=
XM_011541209.1:c.414C=	XP_011539511.1:p.Asn138=
XM_011541210.1:c.414C=	XP_011539512.1:p.Asn138=
XM_011541211.1:c.414C=	XP_011539513.1:p.Asn138=
XM_011541212.1:c.414C=	XP_011539514.1:p.Asn138=
XR_426598.2:n.533C=
XR_946602.1:n.533C=
XR_946603.1:n.533C=
XM_006710559.4:c.414C=	XP_006710622.1:p.Asn138=
XM_006710560.4:c.414C=	XP_006710623.1:p.Asn138=
XM_006710561.4:c.414C=	XP_006710624.1:p.Asn138=
XM_011541209.3:c.414C=	XP_011539511.1:p.Asn138=
XM_011541210.3:c.414C=	XP_011539512.1:p.Asn138=
XM_011541211.3:c.414C=	XP_011539513.1:p.Asn138=
XM_011541212.3:c.414C=	XP_011539514.1:p.Asn138=
XM_017000994.2:c.333C=	XP_016856483.1:p.Asn111=
XM_017000995.2:c.414C=	XP_016856484.1:p.Asn138=
XM_024446315.1:c.279C=	XP_024302083.1:p.Asn93=
XR_001737112.2:n.484C=
XR_001737113.2:n.484C=
XR_002956258.1:n.484C=
XR_426598.4:n.484C=
XR_946602.3:n.484C=
XR_946603.3:n.484C=
NM_015627.3:c.414C= MANE Select	NP_056442.2:p.Asn138=