Canonical Allele Identifier: CA339078715

Gene: LDLRAP1

Linked Data

• MyVariant Identifiers: chr1:g.25883716G>T (hg19) ; chr1:g.25557225G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25557225G>T , CM000663.2:g.25557225G>T	GRCh38
NC_000001.10:g.25883716G>T , CM000663.1:g.25883716G>T	GRCh37
NC_000001.9:g.25756303G>T	NCBI36
NG_008932.1:g.18641G>T , LRG_276:g.18641G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374338.5:c.417G>T MANE Select	ENSP00000363458.4:p.Gln139His
ENST00000374338.4:c.417G>T	ENSP00000363458.4:p.Gln139His
ENST00000462394.1:n.165G>T
ENST00000488127.1:n.887G>T
NM_015627.2:c.417G>T , LRG_276t1:c.417G>T	NP_056442.2:p.Gln139His
XM_006710559.2:c.417G>T	XP_006710622.1:p.Gln139His
XM_006710560.2:c.417G>T	XP_006710623.1:p.Gln139His
XM_006710561.2:c.417G>T	XP_006710624.1:p.Gln139His
XM_011541209.1:c.417G>T	XP_011539511.1:p.Gln139His
XM_011541210.1:c.417G>T	XP_011539512.1:p.Gln139His
XM_011541211.1:c.417G>T	XP_011539513.1:p.Gln139His
XM_011541212.1:c.417G>T	XP_011539514.1:p.Gln139His
XR_426598.2:n.536G>T
XR_946602.1:n.536G>T
XR_946603.1:n.536G>T
XM_006710559.4:c.417G>T	XP_006710622.1:p.Gln139His
XM_006710560.4:c.417G>T	XP_006710623.1:p.Gln139His
XM_006710561.4:c.417G>T	XP_006710624.1:p.Gln139His
XM_011541209.3:c.417G>T	XP_011539511.1:p.Gln139His
XM_011541210.3:c.417G>T	XP_011539512.1:p.Gln139His
XM_011541211.3:c.417G>T	XP_011539513.1:p.Gln139His
XM_011541212.3:c.417G>T	XP_011539514.1:p.Gln139His
XM_017000994.2:c.336G>T	XP_016856483.1:p.Gln112His
XM_017000995.2:c.417G>T	XP_016856484.1:p.Gln139His
XM_024446315.1:c.282G>T	XP_024302083.1:p.Gln94His
XR_001737112.2:n.487G>T
XR_001737113.2:n.487G>T
XR_002956258.1:n.487G>T
XR_426598.4:n.487G>T
XR_946602.3:n.487G>T
XR_946603.3:n.487G>T
NM_015627.3:c.417G>T MANE Select	NP_056442.2:p.Gln139His