Canonical Allele Identifier: CA374964715

Gene: LRSAM1

Linked Data

• ClinVar Variation Id: 540001
• ClinVar RCV Id: RCV000649915
• dbSNP Id: rs1554753670
• MyVariant Identifiers: chr9:g.130219673G>A (hg19) ; chr9:g.127457394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127457394G>A , CM000671.2:g.127457394G>A	GRCh38
NC_000009.11:g.130219673G>A , CM000671.1:g.130219673G>A	GRCh37
NC_000009.10:g.129259494G>A	NCBI36
NG_032008.1:g.10909G>A , LRG_373:g.10909G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.252+1G>A MANE Select	ENSP00000300417.6:n.252+1G>A
ENST00000472068.2:c.238+1G>A	ENSP00000501555.1:n.238+1G>A
ENST00000485704.2:n.687G>A
ENST00000498513.6:c.-496+1G>A	ENSP00000501637.1:n.-496+1G>A
ENST00000674516.1:c.252+1G>A	ENSP00000502441.1:n.252+1G>A
ENST00000674771.1:c.252+1G>A	ENSP00000502627.1:n.252+1G>A
ENST00000674784.1:c.252+1G>A	ENSP00000501837.1:n.252+1G>A
ENST00000674970.1:c.252+1G>A	ENSP00000502493.1:n.252+1G>A
ENST00000675141.1:c.252+1G>A	ENSP00000502420.1:n.252+1G>A
ENST00000675213.1:c.207+1G>A	ENSP00000502218.1:n.207+1G>A
ENST00000675224.1:c.252+1G>A	ENSP00000501869.1:n.252+1G>A
ENST00000675253.1:c.252+1G>A	ENSP00000502557.1:n.252+1G>A
ENST00000675445.1:c.252+1G>A	ENSP00000502253.1:n.252+1G>A
ENST00000675448.1:c.252+1G>A	ENSP00000502167.1:n.252+1G>A
ENST00000675572.1:c.252+1G>A	ENSP00000501598.1:n.252+1G>A
ENST00000675641.1:c.252+1G>A	ENSP00000501845.1:n.252+1G>A
ENST00000675657.1:c.252+1G>A	ENSP00000502002.1:n.252+1G>A
ENST00000675789.1:c.252+1G>A	ENSP00000501954.1:n.252+1G>A
ENST00000675883.1:c.252+1G>A	ENSP00000501592.1:n.252+1G>A
ENST00000675945.1:c.252+1G>A	ENSP00000501835.1:n.252+1G>A
ENST00000676014.1:c.195+1G>A	ENSP00000502058.1:n.195+1G>A
ENST00000676170.1:c.252+1G>A	ENSP00000502177.1:n.252+1G>A
ENST00000676318.1:c.252+1G>A	ENSP00000502300.1:n.252+1G>A
ENST00000676336.1:c.252+1G>A	ENSP00000502686.1:n.252+1G>A
ENST00000676349.1:c.252+1G>A	ENSP00000502155.1:n.252+1G>A
ENST00000300417.10:c.252+1G>A	ENSP00000300417.6:n.252+1G>A
ENST00000323301.8:c.252+1G>A	ENSP00000322937.4:n.252+1G>A
ENST00000373322.1:c.252+1G>A	ENSP00000362419.1:n.252+1G>A
ENST00000373324.8:c.252+1G>A	ENSP00000362421.4:n.252+1G>A
ENST00000485704.1:n.394G>A
NM_001005373.3:c.252+1G>A	NP_001005373.1:n.252+1G>A
NM_001005374.3:c.252+1G>A	NP_001005374.1:n.252+1G>A
NM_001190723.2:c.252+1G>A	NP_001177652.1:n.252+1G>A
NM_138361.5:c.252+1G>A , LRG_373t1:c.252+1G>A	NP_612370.3:n.252+1G>A
XM_006717316.2:c.252+1G>A	XP_006717379.1:n.252+1G>A
XR_929874.1:n.624+1G>A
XM_006717316.4:c.252+1G>A	XP_006717379.1:n.252+1G>A
XM_017015283.1:c.252+1G>A	XP_016870772.1:n.252+1G>A
XM_017015284.2:c.-533+1G>A	XP_016870773.1:n.-533+1G>A
XR_001746415.2:n.606+1G>A
XR_929874.3:n.606+1G>A
NM_001190723.3:c.252+1G>A	NP_001177652.1:n.252+1G>A
NM_001005373.4:c.252+1G>A MANE Select	NP_001005373.1:n.252+1G>A
NM_001005374.4:c.252+1G>A	NP_001005374.1:n.252+1G>A
NM_001384142.1:c.252+1G>A	NP_001371071.1:n.252+1G>A
NM_001384143.1:c.252+1G>A	NP_001371072.1:n.252+1G>A
NM_001384144.1:c.-533+1G>A	NP_001371073.1:n.-533+1G>A
NR_168891.1:n.600+1G>A
NR_168892.1:n.600+1G>A