Canonical Allele Identifier: CA416742378

Gene: LDLRAP1

Linked Data

• gnomAD v4: 1-25557261-G-C
• MyVariant Identifiers: chr1:g.25883752G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557261G>C , CM000663.2:g.25557261G>C	GRCh38
NC_000001.10:g.25883752G>C , CM000663.1:g.25883752G>C	GRCh37
NC_000001.9:g.25756339G>C	NCBI36
NG_008932.1:g.18677G>C , LRG_276:g.18677G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.453G>C MANE Select	ENSP00000363458.4:p.Arg151=
ENST00000374338.4:c.453G>C	ENSP00000363458.4:p.Arg151=
ENST00000462394.1:n.201G>C
ENST00000488127.1:n.923G>C
NM_015627.2:c.453G>C , LRG_276t1:c.453G>C	NP_056442.2:p.Arg151=
XM_006710559.2:c.453G>C	XP_006710622.1:p.Arg151=
XM_006710560.2:c.453G>C	XP_006710623.1:p.Arg151=
XM_006710561.2:c.453G>C	XP_006710624.1:p.Arg151=
XM_011541209.1:c.453G>C	XP_011539511.1:p.Arg151=
XM_011541210.1:c.453G>C	XP_011539512.1:p.Arg151=
XM_011541211.1:c.453G>C	XP_011539513.1:p.Arg151=
XM_011541212.1:c.453G>C	XP_011539514.1:p.Arg151=
XR_426598.2:n.572G>C
XR_946602.1:n.572G>C
XR_946603.1:n.572G>C
XM_006710559.4:c.453G>C	XP_006710622.1:p.Arg151=
XM_006710560.4:c.453G>C	XP_006710623.1:p.Arg151=
XM_006710561.4:c.453G>C	XP_006710624.1:p.Arg151=
XM_011541209.3:c.453G>C	XP_011539511.1:p.Arg151=
XM_011541210.3:c.453G>C	XP_011539512.1:p.Arg151=
XM_011541211.3:c.453G>C	XP_011539513.1:p.Arg151=
XM_011541212.3:c.453G>C	XP_011539514.1:p.Arg151=
XM_017000994.2:c.372G>C	XP_016856483.1:p.Arg124=
XM_017000995.2:c.453G>C	XP_016856484.1:p.Arg151=
XM_024446315.1:c.318G>C	XP_024302083.1:p.Arg106=
XR_001737112.2:n.523G>C
XR_001737113.2:n.523G>C
XR_002956258.1:n.523G>C
XR_426598.4:n.523G>C
XR_946602.3:n.523G>C
XR_946603.3:n.523G>C
NM_015627.3:c.453G>C MANE Select	NP_056442.2:p.Arg151=