Canonical Allele Identifier: CA404098814

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11240242C>T (hg19) ; chr19:g.11129566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11129566C>T , CM000681.2:g.11129566C>T	GRCh38
NC_000019.9:g.11240242C>T , CM000681.1:g.11240242C>T	GRCh37
NC_000019.8:g.11101242C>T	NCBI36
NG_009060.1:g.45186C>T , LRG_274:g.45186C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2701C>T	ENSP00000252444.6:p.Leu901Phe
ENST00000559340.2:c.*512C>T	ENSP00000453696.2:n.*512C>T
ENST00000560467.2:c.2323C>T	ENSP00000453513.2:p.Leu775Phe
ENST00000558518.6:c.2443C>T MANE Select	ENSP00000454071.1:p.Leu815Phe
ENST00000252444.9:c.2697C>T
ENST00000455727.6:c.1939C>T	ENSP00000397829.2:p.Leu647Phe
ENST00000535915.5:c.2320C>T	ENSP00000440520.1:p.Leu774Phe
ENST00000545707.5:c.1909C>T	ENSP00000437639.1:p.Leu637Phe
ENST00000557933.5:c.2505C>T	ENSP00000453557.1:p.Gly835=
ENST00000558013.5:c.2443C>T	ENSP00000453346.1:p.Leu815Phe
ENST00000558518.5:c.2443C>T	ENSP00000454071.1:p.Leu815Phe
ENST00000560628.1:n.108+1912C>T
NM_000527.4:c.2443C>T , LRG_274t1:c.2443C>T	NP_000518.1:p.Leu815Phe
NM_001195798.1:c.2443C>T	NP_001182727.1:p.Leu815Phe
NM_001195799.1:c.2320C>T	NP_001182728.1:p.Leu774Phe
NM_001195800.1:c.1939C>T	NP_001182729.1:p.Leu647Phe
NM_001195803.1:c.1909C>T	NP_001182732.1:p.Leu637Phe
XM_011528010.1:c.2365C>T	XP_011526312.1:p.Leu789Phe
XM_011528011.1:c.2062C>T	XP_011526313.1:p.Leu688Phe
XR_244074.2:n.2453C>T
XM_011528010.2:c.2365C>T	XP_011526312.1:p.Leu789Phe
XR_001753685.2:n.2777C>T
XR_001753686.2:n.2420C>T
NM_000527.5:c.2443C>T MANE Select	NP_000518.1:p.Leu815Phe
NM_001195798.2:c.2443C>T	NP_001182727.1:p.Leu815Phe
NM_001195799.2:c.2320C>T	NP_001182728.1:p.Leu774Phe
NM_001195800.2:c.1939C>T	NP_001182729.1:p.Leu647Phe
NM_001195803.2:c.1909C>T	NP_001182732.1:p.Leu637Phe