Canonical Allele Identifier: CA2841306200

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485688C>G , CM000671.2:g.127485688C>G	GRCh38
NC_000009.11:g.130247967C>G , CM000671.1:g.130247967C>G	GRCh37
NC_000009.10:g.129287788C>G	NCBI36
NG_032008.1:g.39203C>G , LRG_373:g.39203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1160-48C>G MANE Select	ENSP00000300417.6:n.1160-48C>G
ENST00000472068.2:c.*883-48C>G	ENSP00000501555.1:n.*883-48C>G
ENST00000498513.6:c.413-48C>G	ENSP00000501637.1:n.413-48C>G
ENST00000674511.1:n.1035-48C>G
ENST00000674516.1:c.1160-48C>G	ENSP00000502441.1:n.1160-48C>G
ENST00000674621.1:n.1066-48C>G
ENST00000674771.1:c.1160-48C>G	ENSP00000502627.1:n.1160-48C>G
ENST00000674784.1:c.*319-48C>G	ENSP00000501837.1:n.*319-48C>G
ENST00000674970.1:c.*934-48C>G	ENSP00000502493.1:n.*934-48C>G
ENST00000675012.1:n.1040-48C>G
ENST00000675141.1:c.1160-48C>G	ENSP00000502420.1:n.1160-48C>G
ENST00000675198.1:n.1062-48C>G
ENST00000675213.1:c.1115-48C>G	ENSP00000502218.1:n.1115-48C>G
ENST00000675224.1:c.1160-48C>G	ENSP00000501869.1:n.1160-48C>G
ENST00000675253.1:c.1160-48C>G	ENSP00000502557.1:n.1160-48C>G
ENST00000675445.1:c.*832-48C>G	ENSP00000502253.1:n.*832-48C>G
ENST00000675448.1:c.1160-48C>G	ENSP00000502167.1:n.1160-48C>G
ENST00000675521.1:n.1012-48C>G
ENST00000675572.1:c.1160-48C>G	ENSP00000501598.1:n.1160-48C>G
ENST00000675641.1:c.1160-48C>G	ENSP00000501845.1:n.1160-48C>G
ENST00000675657.1:c.1160-48C>G	ENSP00000502002.1:n.1160-48C>G
ENST00000675662.1:n.1053-48C>G
ENST00000675789.1:c.1160-48C>G	ENSP00000501954.1:n.1160-48C>G
ENST00000675883.1:c.1160-48C>G	ENSP00000501592.1:n.1160-48C>G
ENST00000675945.1:c.1160-48C>G	ENSP00000501835.1:n.1160-48C>G
ENST00000676014.1:c.1103-48C>G	ENSP00000502058.1:n.1103-48C>G
ENST00000676035.1:n.921-48C>G
ENST00000676106.1:n.965-48C>G
ENST00000676137.1:n.1051-48C>G
ENST00000676170.1:c.1241-48C>G	ENSP00000502177.1:n.1241-48C>G
ENST00000676318.1:c.1160-48C>G	ENSP00000502300.1:n.1160-48C>G
ENST00000676336.1:c.938-48C>G	ENSP00000502686.1:n.938-48C>G
ENST00000676349.1:c.*929-48C>G	ENSP00000502155.1:n.*929-48C>G
ENST00000676399.1:n.1058-48C>G
ENST00000676409.1:n.1039-48C>G
ENST00000300417.10:c.1160-48C>G	ENSP00000300417.6:n.1160-48C>G
ENST00000323301.8:c.1160-48C>G	ENSP00000322937.4:n.1160-48C>G
ENST00000373322.1:c.1160-48C>G	ENSP00000362419.1:n.1160-48C>G
ENST00000373324.8:c.1160-48C>G	ENSP00000362421.4:n.1160-48C>G
ENST00000472068.1:n.147-48C>G
ENST00000483302.5:n.377-48C>G
ENST00000498513.5:n.413-48C>G
NM_001005373.3:c.1160-48C>G	NP_001005373.1:n.1160-48C>G
NM_001005374.3:c.1160-48C>G	NP_001005374.1:n.1160-48C>G
NM_001190723.2:c.1160-48C>G	NP_001177652.1:n.1160-48C>G
NM_138361.5:c.1160-48C>G , LRG_373t1:c.1160-48C>G	NP_612370.3:n.1160-48C>G
XM_006717316.2:c.1160-48C>G	XP_006717379.1:n.1160-48C>G
XR_929874.1:n.1532-48C>G
XM_006717316.4:c.1160-48C>G	XP_006717379.1:n.1160-48C>G
XM_017015283.1:c.1160-48C>G	XP_016870772.1:n.1160-48C>G
XM_017015284.2:c.371-48C>G	XP_016870773.1:n.371-48C>G
XR_001746415.2:n.1514-48C>G
XR_929874.3:n.1514-48C>G
NM_001190723.3:c.1160-48C>G	NP_001177652.1:n.1160-48C>G
NM_001005373.4:c.1160-48C>G MANE Select	NP_001005373.1:n.1160-48C>G
NM_001005374.4:c.1160-48C>G	NP_001005374.1:n.1160-48C>G
NM_001384142.1:c.1160-48C>G	NP_001371071.1:n.1160-48C>G
NM_001384143.1:c.1160-48C>G	NP_001371072.1:n.1160-48C>G
NM_001384144.1:c.371-48C>G	NP_001371073.1:n.371-48C>G
NR_168891.1:n.1508-48C>G
NR_168892.1:n.1508-48C>G