Canonical Allele Identifier: CA1159697441

Gene: LDLRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25553921G= , CM000663.2:g.25553921G=	GRCh38
NC_000001.10:g.25880412G= , CM000663.1:g.25880412G=	GRCh37
NC_000001.9:g.25752999G=	NCBI36
NG_008932.1:g.15337G= , LRG_276:g.15337G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.89-1G= MANE Select	ENSP00000363458.4:n.89-1G=
ENST00000374338.4:c.89-1G=	ENSP00000363458.4:n.89-1G=
ENST00000485476.2:n.76-1G=
ENST00000488127.1:n.558G=
NM_015627.2:c.89-1G= , LRG_276t1:c.89-1G=	NP_056442.2:n.89-1G=
XM_006710559.2:c.89-1G=	XP_006710622.1:n.89-1G=
XM_006710560.2:c.89-1G=	XP_006710623.1:n.89-1G=
XM_006710561.2:c.89-1G=	XP_006710624.1:n.89-1G=
XM_011541209.1:c.89-1G=	XP_011539511.1:n.89-1G=
XM_011541210.1:c.89-1G=	XP_011539512.1:n.89-1G=
XM_011541211.1:c.89-1G=	XP_011539513.1:n.89-1G=
XM_011541212.1:c.89-1G=	XP_011539514.1:n.89-1G=
XR_426598.2:n.208-1G=
XR_946602.1:n.208-1G=
XR_946603.1:n.208-1G=
XM_006710559.4:c.89-1G=	XP_006710622.1:n.89-1G=
XM_006710560.4:c.89-1G=	XP_006710623.1:n.89-1G=
XM_006710561.4:c.89-1G=	XP_006710624.1:n.89-1G=
XM_011541209.3:c.89-1G=	XP_011539511.1:n.89-1G=
XM_011541210.3:c.89-1G=	XP_011539512.1:n.89-1G=
XM_011541211.3:c.89-1G=	XP_011539513.1:n.89-1G=
XM_011541212.3:c.89-1G=	XP_011539514.1:n.89-1G=
XM_017000994.2:c.8-1G=	XP_016856483.1:n.8-1G=
XM_017000995.2:c.89-1G=	XP_016856484.1:n.89-1G=
XM_024446315.1:c.-47-1G=	XP_024302083.1:n.-47-1G=
XR_001737112.2:n.159-1G=
XR_001737113.2:n.159-1G=
XR_002956258.1:n.159-1G=
XR_426598.4:n.159-1G=
XR_946602.3:n.159-1G=
XR_946603.3:n.159-1G=
NM_015627.3:c.89-1G= MANE Select	NP_056442.2:n.89-1G=