Canonical Allele Identifier: CA372785838

Gene: VLDLR VLDLR-AS1

Linked Data

• gnomAD v4: 9-2622273-T-C
• MyVariant Identifiers: chr9:g.2622273T>C (hg19) ; chr9:g.2622273T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2622273T>C , CM000671.2:g.2622273T>C	GRCh38
NC_000009.11:g.2622273T>C , CM000671.1:g.2622273T>C	GRCh37
NC_000009.10:g.2612273T>C	NCBI36
NG_012741.1:g.5481T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382096.6:c.82+2T>C (VLDLR)	ENSP00000371528.2:n.82+2T>C
ENST00000382100.8:c.82+2T>C (VLDLR) MANE Select	ENSP00000371532.2:n.82+2T>C
ENST00000679851.1:n.67+2T>C (VLDLR)
ENST00000680243.1:c.82+2T>C (VLDLR)	ENSP00000505911.1:n.82+2T>C
ENST00000680746.1:c.82+2T>C (VLDLR)	ENSP00000505030.1:n.82+2T>C
ENST00000680891.1:c.82+2T>C (VLDLR)	ENSP00000505167.1:n.82+2T>C
ENST00000681306.1:c.82+2T>C (VLDLR)	ENSP00000506072.1:n.82+2T>C
ENST00000681618.1:c.82+2T>C (VLDLR)	ENSP00000505773.1:n.82+2T>C
ENST00000681644.1:c.82+2T>C (VLDLR)	ENSP00000505180.1:n.82+2T>C
ENST00000681770.1:n.70+2T>C (VLDLR)
ENST00000681806.1:c.82+2T>C (VLDLR)	ENSP00000505282.1:n.82+2T>C
ENST00000382096.5:c.82+2T>C (VLDLR)	ENSP00000371528.1:n.82+2T>C
ENST00000382099.2:c.82+2T>C (VLDLR)	ENSP00000371531.2:n.82+2T>C
ENST00000382100.7:c.82+2T>C (VLDLR)	ENSP00000371532.2:n.82+2T>C
NM_001018056.1:c.82+2T>C (VLDLR)	NP_001018066.1:n.82+2T>C
NM_003383.3:c.82+2T>C (VLDLR)	NP_003374.3:n.82+2T>C
NR_015375.2:n.101A>G (VLDLR-AS1)
XM_011518029.1:c.82+2T>C (VLDLR)	XP_011516331.1:n.82+2T>C
NM_001018056.2:c.82+2T>C (VLDLR)	NP_001018066.1:n.82+2T>C
NM_001322225.1:c.82+2T>C (VLDLR)	NP_001309154.1:n.82+2T>C
NM_001322226.1:c.82+2T>C (VLDLR)	NP_001309155.1:n.82+2T>C
NM_003383.4:c.82+2T>C (VLDLR)	NP_003374.3:n.82+2T>C
XR_001746373.2:n.486+2T>C (VLDLR)
XR_002956805.1:n.486+2T>C (VLDLR)
NM_003383.5:c.82+2T>C (VLDLR) MANE Select	NP_003374.3:n.82+2T>C
NM_001018056.3:c.82+2T>C (VLDLR)	NP_001018066.1:n.82+2T>C
NM_001322225.2:c.82+2T>C (VLDLR)	NP_001309154.1:n.82+2T>C
NM_001322226.2:c.82+2T>C (VLDLR)	NP_001309155.1:n.82+2T>C