Canonical Allele Identifier: CA404093934

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11231164G>T (hg19) ; chr19:g.11120488G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120488G>T , CM000681.2:g.11120488G>T	GRCh38
NC_000019.9:g.11231164G>T , CM000681.1:g.11231164G>T	GRCh37
NC_000019.8:g.11092164G>T	NCBI36
NG_009060.1:g.36108G>T , LRG_274:g.36108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2364G>T	ENSP00000252444.6:p.Met788Ile
ENST00000559340.2:c.*175G>T	ENSP00000453696.2:n.*175G>T
ENST00000560467.2:c.1986G>T	ENSP00000453513.2:p.Met662Ile
ENST00000558518.6:c.2106G>T MANE Select	ENSP00000454071.1:p.Met702Ile
ENST00000252444.9:c.2360G>T
ENST00000455727.6:c.1602G>T	ENSP00000397829.2:p.Met534Ile
ENST00000535915.5:c.1983G>T	ENSP00000440520.1:p.Met661Ile
ENST00000545707.5:c.1606+255G>T	ENSP00000437639.1:n.1606+255G>T
ENST00000557933.5:c.2106G>T	ENSP00000453557.1:p.Met702Ile
ENST00000558013.5:c.2106G>T	ENSP00000453346.1:p.Met702Ile
ENST00000558518.5:c.2106G>T	ENSP00000454071.1:p.Met702Ile
NM_000527.4:c.2106G>T , LRG_274t1:c.2106G>T	NP_000518.1:p.Met702Ile
NM_001195798.1:c.2106G>T	NP_001182727.1:p.Met702Ile
NM_001195799.1:c.1983G>T	NP_001182728.1:p.Met661Ile
NM_001195800.1:c.1602G>T	NP_001182729.1:p.Met534Ile
NM_001195803.1:c.1606+255G>T	NP_001182732.1:n.1606+255G>T
XM_011528010.1:c.2106G>T	XP_011526312.1:p.Met702Ile
XM_011528011.1:c.1725G>T	XP_011526313.1:p.Met575Ile
XR_244074.2:n.2116G>T
XM_011528010.2:c.2106G>T	XP_011526312.1:p.Met702Ile
XR_001753685.2:n.2223G>T
XR_001753686.2:n.2083G>T
NM_000527.5:c.2106G>T MANE Select	NP_000518.1:p.Met702Ile
NM_001195798.2:c.2106G>T	NP_001182727.1:p.Met702Ile
NM_001195799.2:c.1983G>T	NP_001182728.1:p.Met661Ile
NM_001195800.2:c.1602G>T	NP_001182729.1:p.Met534Ile
NM_001195803.2:c.1606+255G>T	NP_001182732.1:n.1606+255G>T