Canonical Allele Identifier: CA404093182

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11230878G>T (hg19) ; chr19:g.11120202G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120202G>T , CM000681.2:g.11120202G>T	GRCh38
NC_000019.9:g.11230878G>T , CM000681.1:g.11230878G>T	GRCh37
NC_000019.8:g.11091878G>T	NCBI36
NG_009060.1:g.35822G>T , LRG_274:g.35822G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2214G>T	ENSP00000252444.6:p.Met738Ile
ENST00000559340.2:c.*25G>T	ENSP00000453696.2:n.*25G>T
ENST00000560467.2:c.1836G>T	ENSP00000453513.2:p.Met612Ile
ENST00000558518.6:c.1956G>T MANE Select	ENSP00000454071.1:p.Met652Ile
ENST00000252444.9:c.2210G>T
ENST00000455727.6:c.1452G>T	ENSP00000397829.2:p.Met484Ile
ENST00000535915.5:c.1833G>T	ENSP00000440520.1:p.Met611Ile
ENST00000545707.5:c.1575G>T	ENSP00000437639.1:p.Met525Ile
ENST00000557933.5:c.1956G>T	ENSP00000453557.1:p.Met652Ile
ENST00000558013.5:c.1956G>T	ENSP00000453346.1:p.Met652Ile
ENST00000558518.5:c.1956G>T	ENSP00000454071.1:p.Met652Ile
ENST00000559340.1:c.537G>T
NM_000527.4:c.1956G>T , LRG_274t1:c.1956G>T	NP_000518.1:p.Met652Ile
NM_001195798.1:c.1956G>T	NP_001182727.1:p.Met652Ile
NM_001195799.1:c.1833G>T	NP_001182728.1:p.Met611Ile
NM_001195800.1:c.1452G>T	NP_001182729.1:p.Met484Ile
NM_001195803.1:c.1575G>T	NP_001182732.1:p.Met525Ile
XM_011528010.1:c.1956G>T	XP_011526312.1:p.Met652Ile
XM_011528011.1:c.1575G>T	XP_011526313.1:p.Met525Ile
XR_244074.2:n.1966G>T
XM_011528010.2:c.1956G>T	XP_011526312.1:p.Met652Ile
XR_001753685.2:n.2073G>T
XR_001753686.2:n.1933G>T
NM_000527.5:c.1956G>T MANE Select	NP_000518.1:p.Met652Ile
NM_001195798.2:c.1956G>T	NP_001182727.1:p.Met652Ile
NM_001195799.2:c.1833G>T	NP_001182728.1:p.Met611Ile
NM_001195800.2:c.1452G>T	NP_001182729.1:p.Met484Ile
NM_001195803.2:c.1575G>T	NP_001182732.1:p.Met525Ile