Canonical Allele Identifier: CA1141580676

Gene: LDLRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557214C= , CM000663.2:g.25557214C=	GRCh38
NC_000001.10:g.25883705C= , CM000663.1:g.25883705C=	GRCh37
NC_000001.9:g.25756292C=	NCBI36
NG_008932.1:g.18630C= , LRG_276:g.18630C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.406C= MANE Select	ENSP00000363458.4:p.Gln136=
ENST00000374338.4:c.406C=	ENSP00000363458.4:p.Gln136=
ENST00000462394.1:n.154C=
ENST00000488127.1:n.876C=
NM_015627.2:c.406C= , LRG_276t1:c.406C=	NP_056442.2:p.Gln136=
XM_006710559.2:c.406C=	XP_006710622.1:p.Gln136=
XM_006710560.2:c.406C=	XP_006710623.1:p.Gln136=
XM_006710561.2:c.406C=	XP_006710624.1:p.Gln136=
XM_011541209.1:c.406C=	XP_011539511.1:p.Gln136=
XM_011541210.1:c.406C=	XP_011539512.1:p.Gln136=
XM_011541211.1:c.406C=	XP_011539513.1:p.Gln136=
XM_011541212.1:c.406C=	XP_011539514.1:p.Gln136=
XR_426598.2:n.525C=
XR_946602.1:n.525C=
XR_946603.1:n.525C=
XM_006710559.4:c.406C=	XP_006710622.1:p.Gln136=
XM_006710560.4:c.406C=	XP_006710623.1:p.Gln136=
XM_006710561.4:c.406C=	XP_006710624.1:p.Gln136=
XM_011541209.3:c.406C=	XP_011539511.1:p.Gln136=
XM_011541210.3:c.406C=	XP_011539512.1:p.Gln136=
XM_011541211.3:c.406C=	XP_011539513.1:p.Gln136=
XM_011541212.3:c.406C=	XP_011539514.1:p.Gln136=
XM_017000994.2:c.325C=	XP_016856483.1:p.Gln109=
XM_017000995.2:c.406C=	XP_016856484.1:p.Gln136=
XM_024446315.1:c.271C=	XP_024302083.1:p.Gln91=
XR_001737112.2:n.476C=
XR_001737113.2:n.476C=
XR_002956258.1:n.476C=
XR_426598.4:n.476C=
XR_946602.3:n.476C=
XR_946603.3:n.476C=
NM_015627.3:c.406C= MANE Select	NP_056442.2:p.Gln136=