Canonical Allele Identifier: CA1145541149

Gene: LDLRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557243C= , CM000663.2:g.25557243C=	GRCh38
NC_000001.10:g.25883734C= , CM000663.1:g.25883734C=	GRCh37
NC_000001.9:g.25756321C=	NCBI36
NG_008932.1:g.18659C= , LRG_276:g.18659C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.435C= MANE Select	ENSP00000363458.4:p.Ala145=
ENST00000374338.4:c.435C=	ENSP00000363458.4:p.Ala145=
ENST00000462394.1:n.183C=
ENST00000488127.1:n.905C=
NM_015627.2:c.435C= , LRG_276t1:c.435C=	NP_056442.2:p.Ala145=
XM_006710559.2:c.435C=	XP_006710622.1:p.Ala145=
XM_006710560.2:c.435C=	XP_006710623.1:p.Ala145=
XM_006710561.2:c.435C=	XP_006710624.1:p.Ala145=
XM_011541209.1:c.435C=	XP_011539511.1:p.Ala145=
XM_011541210.1:c.435C=	XP_011539512.1:p.Ala145=
XM_011541211.1:c.435C=	XP_011539513.1:p.Ala145=
XM_011541212.1:c.435C=	XP_011539514.1:p.Ala145=
XR_426598.2:n.554C=
XR_946602.1:n.554C=
XR_946603.1:n.554C=
XM_006710559.4:c.435C=	XP_006710622.1:p.Ala145=
XM_006710560.4:c.435C=	XP_006710623.1:p.Ala145=
XM_006710561.4:c.435C=	XP_006710624.1:p.Ala145=
XM_011541209.3:c.435C=	XP_011539511.1:p.Ala145=
XM_011541210.3:c.435C=	XP_011539512.1:p.Ala145=
XM_011541211.3:c.435C=	XP_011539513.1:p.Ala145=
XM_011541212.3:c.435C=	XP_011539514.1:p.Ala145=
XM_017000994.2:c.354C=	XP_016856483.1:p.Ala118=
XM_017000995.2:c.435C=	XP_016856484.1:p.Ala145=
XM_024446315.1:c.300C=	XP_024302083.1:p.Ala100=
XR_001737112.2:n.505C=
XR_001737113.2:n.505C=
XR_002956258.1:n.505C=
XR_426598.4:n.505C=
XR_946602.3:n.505C=
XR_946603.3:n.505C=
NM_015627.3:c.435C= MANE Select	NP_056442.2:p.Ala145=