Canonical Allele Identifier: CA5247077

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127495322G>A , CM000671.2:g.127495322G>A	GRCh38
NC_000009.11:g.130257601G>A , CM000671.1:g.130257601G>A	GRCh37
NC_000009.10:g.129297422G>A	NCBI36
NG_032008.1:g.48837G>A , LRG_373:g.48837G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.1602G>A MANE Select	NP_001005373.1:p.Thr534=
ENST00000300417.11:c.1602G>A MANE Select	ENSP00000300417.6:p.Thr534=
NM_001005373.3:c.1602G>A	NP_001005373.1:p.Thr534=
NM_001005374.3:c.1602G>A	NP_001005374.1:p.Thr534=
NM_001005374.4:c.1602G>A	NP_001005374.1:p.Thr534=
NM_001190723.2:c.1521G>A	NP_001177652.1:p.Thr507=
NM_001190723.3:c.1521G>A	NP_001177652.1:p.Thr507=
NM_001384142.1:c.1602G>A	NP_001371071.1:p.Thr534=
NM_001384143.1:c.1600-642G>A	NP_001371072.1:n.1600-642G>A
NM_001384144.1:c.813G>A	NP_001371073.1:p.Thr271=
NM_138361.5:c.1602G>A , LRG_373t1:c.1602G>A	NP_612370.3:p.Thr534=
NR_168891.1:n.2131G>A
NR_168892.1:n.1955G>A
ENST00000300417.10:c.1602G>A	ENSP00000300417.6:p.Thr534=
ENST00000323301.8:c.1602G>A	ENSP00000322937.4:p.Thr534=
ENST00000373322.1:c.1602G>A	ENSP00000362419.1:p.Thr534=
ENST00000373324.8:c.1521G>A	ENSP00000362421.4:p.Thr507=
ENST00000472068.1:n.592-642G>A
ENST00000472068.2:c.*1330G>A	ENSP00000501555.1:n.*1330G>A
ENST00000483302.5:n.824G>A
ENST00000483302.6:n.2267G>A
ENST00000498513.6:c.*493G>A	ENSP00000501637.1:n.*493G>A
ENST00000674511.1:n.1298-642G>A
ENST00000674516.1:c.1602G>A	ENSP00000502441.1:p.Thr534=
ENST00000674621.1:n.1652G>A
ENST00000674771.1:c.*342-642G>A	ENSP00000502627.1:n.*342-642G>A
ENST00000674784.1:c.*759-642G>A	ENSP00000501837.1:n.*759-642G>A
ENST00000674970.1:c.*1376G>A	ENSP00000502493.1:n.*1376G>A
ENST00000675012.1:n.1546G>A
ENST00000675141.1:c.1600-642G>A	ENSP00000502420.1:n.1600-642G>A
ENST00000675198.1:n.1482G>A
ENST00000675213.1:c.1557G>A	ENSP00000502218.1:p.Thr519=
ENST00000675224.1:c.1602G>A	ENSP00000501869.1:p.Thr534=
ENST00000675253.1:c.*371-642G>A	ENSP00000502557.1:n.*371-642G>A
ENST00000675445.1:c.*1274G>A	ENSP00000502253.1:n.*1274G>A
ENST00000675448.1:c.1602G>A	ENSP00000502167.1:p.Thr534=
ENST00000675521.1:n.1512G>A
ENST00000675572.1:c.1600-642G>A	ENSP00000501598.1:n.1600-642G>A
ENST00000675641.1:c.*344G>A	ENSP00000501845.1:n.*344G>A
ENST00000675657.1:c.*215G>A	ENSP00000502002.1:n.*215G>A
ENST00000675662.1:n.1397G>A
ENST00000675789.1:c.1519-642G>A	ENSP00000501954.1:n.1519-642G>A
ENST00000675883.1:c.1521G>A	ENSP00000501592.1:p.Thr507=
ENST00000675945.1:c.*422-642G>A	ENSP00000501835.1:n.*422-642G>A
ENST00000676014.1:c.1545G>A	ENSP00000502058.1:p.Thr515=
ENST00000676035.1:n.1361-642G>A
ENST00000676106.1:n.1736-642G>A
ENST00000676137.1:n.1632G>A
ENST00000676170.1:c.1683G>A	ENSP00000502177.1:p.Thr561=
ENST00000676318.1:c.*2432G>A	ENSP00000502300.1:n.*2432G>A
ENST00000676336.1:c.*215G>A	ENSP00000502686.1:n.*215G>A
ENST00000676349.1:c.*1290G>A	ENSP00000502155.1:n.*1290G>A
ENST00000676399.1:n.1505G>A
ENST00000676409.1:n.1662G>A
XM_006717316.2:c.1600-642G>A	XP_006717379.1:n.1600-642G>A
XM_006717316.4:c.1600-642G>A	XP_006717379.1:n.1600-642G>A
XM_017015283.1:c.1602G>A	XP_016870772.1:p.Thr534=
XM_017015284.2:c.813G>A	XP_016870773.1:p.Thr271=
XR_001746415.2:n.2137G>A
XR_929874.3:n.1961G>A