Canonical Allele Identifier: CA2322773656

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11116882T= , CM000681.2:g.11116882T=	GRCh38
NC_000019.9:g.11227558T= , CM000681.1:g.11227558T=	GRCh37
NC_000019.8:g.11088558T=	NCBI36
NG_009060.1:g.32502T= , LRG_274:g.32502T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1987T=	ENSP00000252444.6:p.Trp663=
ENST00000559340.2:c.1705+670T=	ENSP00000453696.2:n.1705+670T=
ENST00000560467.2:c.1609T=	ENSP00000453513.2:p.Trp537=
ENST00000558518.6:c.1729T= MANE Select	ENSP00000454071.1:p.Trp577=
ENST00000252444.9:c.1983T=
ENST00000455727.6:c.1225T=	ENSP00000397829.2:p.Trp409=
ENST00000535915.5:c.1606T=	ENSP00000440520.1:p.Trp536=
ENST00000545707.5:c.1348T=	ENSP00000437639.1:p.Trp450=
ENST00000557933.5:c.1729T=	ENSP00000453557.1:p.Trp577=
ENST00000558013.5:c.1729T=	ENSP00000453346.1:p.Trp577=
ENST00000558518.5:c.1729T=	ENSP00000454071.1:p.Trp577=
ENST00000559340.1:c.426+670T=
NM_000527.4:c.1729T= , LRG_274t1:c.1729T=	NP_000518.1:p.Trp577=
NM_001195798.1:c.1729T=	NP_001182727.1:p.Trp577=
NM_001195799.1:c.1606T=	NP_001182728.1:p.Trp536=
NM_001195800.1:c.1225T=	NP_001182729.1:p.Trp409=
NM_001195803.1:c.1348T=	NP_001182732.1:p.Trp450=
XM_011528010.1:c.1729T=	XP_011526312.1:p.Trp577=
XM_011528011.1:c.1348T=	XP_011526313.1:p.Trp450=
XR_244074.2:n.1855+670T=
XM_011528010.2:c.1729T=	XP_011526312.1:p.Trp577=
XR_001753685.2:n.1846T=
XR_001753686.2:n.1822+670T=
NM_000527.5:c.1729T= MANE Select	NP_000518.1:p.Trp577=
NM_001195798.2:c.1729T=	NP_001182727.1:p.Trp577=
NM_001195799.2:c.1606T=	NP_001182728.1:p.Trp536=
NM_001195800.2:c.1225T=	NP_001182729.1:p.Trp409=
NM_001195803.2:c.1348T=	NP_001182732.1:p.Trp450=