Canonical Allele Identifier: CA199852959

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1009481183
• gnomAD v3: 9-127501021-C-T
• gnomAD v4: 9-127501021-C-T
• MyVariant Identifiers: chr9:g.130263300C>T (hg19) ; chr9:g.127501021C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501021C>T , CM000671.2:g.127501021C>T	GRCh38
NC_000009.11:g.130263300C>T , CM000671.1:g.130263300C>T	GRCh37
NC_000009.10:g.129303121C>T	NCBI36
NG_032008.1:g.54536C>T , LRG_373:g.54536C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1924C>T MANE Select	ENSP00000300417.6:p.Pro642Ser
ENST00000472068.2:c.*1648C>T	ENSP00000501555.1:n.*1648C>T
ENST00000483302.6:n.2589C>T
ENST00000498513.6:c.*815C>T	ENSP00000501637.1:n.*815C>T
ENST00000674511.1:n.1523C>T
ENST00000674516.1:c.*540C>T	ENSP00000502441.1:n.*540C>T
ENST00000674621.1:n.1861-2352C>T
ENST00000674771.1:c.*567C>T	ENSP00000502627.1:n.*567C>T
ENST00000674784.1:c.*984C>T	ENSP00000501837.1:n.*984C>T
ENST00000674970.1:c.*1698C>T	ENSP00000502493.1:n.*1698C>T
ENST00000675012.1:n.1868C>T
ENST00000675141.1:c.1825C>T	ENSP00000502420.1:p.Pro609Ser
ENST00000675198.1:n.1804C>T
ENST00000675213.1:c.1879C>T	ENSP00000502218.1:p.Pro627Ser
ENST00000675224.1:c.1952C>T	ENSP00000501869.1:p.Thr651Ile
ENST00000675253.1:c.*596C>T	ENSP00000502557.1:n.*596C>T
ENST00000675445.1:c.*1596C>T	ENSP00000502253.1:n.*1596C>T
ENST00000675448.1:c.1924C>T	ENSP00000502167.1:p.Pro642Ser
ENST00000675521.1:n.1834C>T
ENST00000675572.1:c.1825C>T	ENSP00000501598.1:p.Pro609Ser
ENST00000675641.1:c.*666C>T	ENSP00000501845.1:n.*666C>T
ENST00000675657.1:c.*537C>T	ENSP00000502002.1:n.*537C>T
ENST00000675662.1:n.1719C>T
ENST00000675789.1:c.1744C>T	ENSP00000501954.1:p.Pro582Ser
ENST00000675883.1:c.1843C>T	ENSP00000501592.1:p.Pro615Ser
ENST00000675945.1:c.*565C>T	ENSP00000501835.1:n.*565C>T
ENST00000676014.1:c.1867C>T	ENSP00000502058.1:p.Pro623Ser
ENST00000676035.1:n.1586C>T
ENST00000676106.1:n.1961C>T
ENST00000676137.1:n.1954C>T
ENST00000676170.1:c.2005C>T	ENSP00000502177.1:p.Pro669Ser
ENST00000676318.1:c.*2754C>T	ENSP00000502300.1:n.*2754C>T
ENST00000676336.1:c.*537C>T	ENSP00000502686.1:n.*537C>T
ENST00000676349.1:c.*1612C>T	ENSP00000502155.1:n.*1612C>T
ENST00000676399.1:n.1827C>T
ENST00000676409.1:n.1984C>T
ENST00000300417.10:c.1924C>T	ENSP00000300417.6:p.Pro642Ser
ENST00000323301.8:c.1924C>T	ENSP00000322937.4:p.Pro642Ser
ENST00000373322.1:c.1924C>T	ENSP00000362419.1:p.Pro642Ser
ENST00000373324.8:c.1843C>T	ENSP00000362421.4:p.Pro615Ser
ENST00000472068.1:n.817C>T
ENST00000483302.5:n.1146C>T
NM_001005373.3:c.1924C>T	NP_001005373.1:p.Pro642Ser
NM_001005374.3:c.1924C>T	NP_001005374.1:p.Pro642Ser
NM_001190723.2:c.1843C>T	NP_001177652.1:p.Pro615Ser
NM_138361.5:c.1924C>T , LRG_373t1:c.1924C>T	NP_612370.3:p.Pro642Ser
XM_006717316.2:c.1825C>T	XP_006717379.1:p.Pro609Ser
XM_006717316.4:c.1825C>T	XP_006717379.1:p.Pro609Ser
XM_017015283.1:c.1924C>T	XP_016870772.1:p.Pro642Ser
XM_017015284.2:c.1135C>T	XP_016870773.1:p.Pro379Ser
XR_001746415.2:n.2459C>T
XR_929874.3:n.2283C>T
NM_001190723.3:c.1843C>T	NP_001177652.1:p.Pro615Ser
NM_001005373.4:c.1924C>T MANE Select	NP_001005373.1:p.Pro642Ser
NM_001005374.4:c.1924C>T	NP_001005374.1:p.Pro642Ser
NM_001384142.1:c.1924C>T	NP_001371071.1:p.Pro642Ser
NM_001384143.1:c.1825C>T	NP_001371072.1:p.Pro609Ser
NM_001384144.1:c.1135C>T	NP_001371073.1:p.Pro379Ser
NR_168891.1:n.2453C>T
NR_168892.1:n.2277C>T