Canonical Allele Identifier: CA783240680

Gene: LDLR SPC24

Linked Data

• dbSNP Id: rs1433099
• gnomAD v3: 19-11131982-T-A
• gnomAD v4: 19-11131982-T-A
• MyVariant Identifiers: chr19:g.11242658T>A (hg19) ; chr19:g.11131982T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11131982T>A , CM000681.2:g.11131982T>A	GRCh38
NC_000019.9:g.11242658T>A , CM000681.1:g.11242658T>A	GRCh37
NC_000019.8:g.11103658T>A	NCBI36
NG_009060.1:g.47602T>A , LRG_274:g.47602T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.*666T>A (LDLR)	ENSP00000252444.6:n.*666T>A
ENST00000559340.2:c.*1318T>A (LDLR)	ENSP00000453696.2:n.*1318T>A
ENST00000560467.2:c.*666T>A (LDLR)	ENSP00000453513.2:n.*666T>A
ENST00000558518.6:c.*666T>A (LDLR) MANE Select	ENSP00000454071.1:n.*666T>A
ENST00000252444.9:c.3503T>A (LDLR)
ENST00000558518.5:c.*666T>A (LDLR)	ENSP00000454071.1:n.*666T>A
ENST00000560628.1:n.109-1113T>A (LDLR)
ENST00000585567.5:c.540-375A>T (SPC24)	ENSP00000468818.1:n.540-375A>T
NM_000527.4:c.*666T>A , LRG_274t1:c.*666T>A (LDLR)	NP_000518.1:n.*666T>A
NM_001195798.1:c.*666T>A (LDLR)	NP_001182727.1:n.*666T>A
NM_001195799.1:c.*666T>A (LDLR)	NP_001182728.1:n.*666T>A
NM_001195800.1:c.*666T>A (LDLR)	NP_001182729.1:n.*666T>A
NM_001195803.1:c.*666T>A (LDLR)	NP_001182732.1:n.*666T>A
XM_011528010.1:c.*666T>A (LDLR)	XP_011526312.1:n.*666T>A
XM_011528011.1:c.*666T>A (LDLR)	XP_011526313.1:n.*666T>A
XM_011528010.2:c.*666T>A (LDLR)	XP_011526312.1:n.*666T>A
XR_001753685.2:n.3583T>A (LDLR)
XR_001753686.2:n.3226T>A (LDLR)
NM_000527.5:c.*666T>A (LDLR) MANE Select	NP_000518.1:n.*666T>A
NM_001195798.2:c.*666T>A (LDLR)	NP_001182727.1:n.*666T>A
NM_001195799.2:c.*666T>A (LDLR)	NP_001182728.1:n.*666T>A
NM_001195800.2:c.*666T>A (LDLR)	NP_001182729.1:n.*666T>A
NM_001195803.2:c.*666T>A (LDLR)	NP_001182732.1:n.*666T>A