Canonical Allele Identifier: CA467236619

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263299A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501020A>T , CM000671.2:g.127501020A>T	GRCh38
NC_000009.11:g.130263299A>T , CM000671.1:g.130263299A>T	GRCh37
NC_000009.10:g.129303120A>T	NCBI36
NG_032008.1:g.54535A>T , LRG_373:g.54535A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1923A>T MANE Select	ENSP00000300417.6:p.Pro641=
ENST00000472068.2:c.*1647A>T	ENSP00000501555.1:n.*1647A>T
ENST00000483302.6:n.2588A>T
ENST00000498513.6:c.*814A>T	ENSP00000501637.1:n.*814A>T
ENST00000674511.1:n.1522A>T
ENST00000674516.1:c.*539A>T	ENSP00000502441.1:n.*539A>T
ENST00000674621.1:n.1861-2353A>T
ENST00000674771.1:c.*566A>T	ENSP00000502627.1:n.*566A>T
ENST00000674784.1:c.*983A>T	ENSP00000501837.1:n.*983A>T
ENST00000674970.1:c.*1697A>T	ENSP00000502493.1:n.*1697A>T
ENST00000675012.1:n.1867A>T
ENST00000675141.1:c.1824A>T	ENSP00000502420.1:p.Pro608=
ENST00000675198.1:n.1803A>T
ENST00000675213.1:c.1878A>T	ENSP00000502218.1:p.Pro626=
ENST00000675224.1:c.1951A>T	ENSP00000501869.1:p.Thr651Ser
ENST00000675253.1:c.*595A>T	ENSP00000502557.1:n.*595A>T
ENST00000675445.1:c.*1595A>T	ENSP00000502253.1:n.*1595A>T
ENST00000675448.1:c.1923A>T	ENSP00000502167.1:p.Pro641=
ENST00000675521.1:n.1833A>T
ENST00000675572.1:c.1824A>T	ENSP00000501598.1:p.Pro608=
ENST00000675641.1:c.*665A>T	ENSP00000501845.1:n.*665A>T
ENST00000675657.1:c.*536A>T	ENSP00000502002.1:n.*536A>T
ENST00000675662.1:n.1718A>T
ENST00000675789.1:c.1743A>T	ENSP00000501954.1:p.Pro581=
ENST00000675883.1:c.1842A>T	ENSP00000501592.1:p.Pro614=
ENST00000675945.1:c.*564A>T	ENSP00000501835.1:n.*564A>T
ENST00000676014.1:c.1866A>T	ENSP00000502058.1:p.Pro622=
ENST00000676035.1:n.1585A>T
ENST00000676106.1:n.1960A>T
ENST00000676137.1:n.1953A>T
ENST00000676170.1:c.2004A>T	ENSP00000502177.1:p.Pro668=
ENST00000676318.1:c.*2753A>T	ENSP00000502300.1:n.*2753A>T
ENST00000676336.1:c.*536A>T	ENSP00000502686.1:n.*536A>T
ENST00000676349.1:c.*1611A>T	ENSP00000502155.1:n.*1611A>T
ENST00000676399.1:n.1826A>T
ENST00000676409.1:n.1983A>T
ENST00000300417.10:c.1923A>T	ENSP00000300417.6:p.Pro641=
ENST00000323301.8:c.1923A>T	ENSP00000322937.4:p.Pro641=
ENST00000373322.1:c.1923A>T	ENSP00000362419.1:p.Pro641=
ENST00000373324.8:c.1842A>T	ENSP00000362421.4:p.Pro614=
ENST00000472068.1:n.816A>T
ENST00000483302.5:n.1145A>T
NM_001005373.3:c.1923A>T	NP_001005373.1:p.Pro641=
NM_001005374.3:c.1923A>T	NP_001005374.1:p.Pro641=
NM_001190723.2:c.1842A>T	NP_001177652.1:p.Pro614=
NM_138361.5:c.1923A>T , LRG_373t1:c.1923A>T	NP_612370.3:p.Pro641=
XM_006717316.2:c.1824A>T	XP_006717379.1:p.Pro608=
XM_006717316.4:c.1824A>T	XP_006717379.1:p.Pro608=
XM_017015283.1:c.1923A>T	XP_016870772.1:p.Pro641=
XM_017015284.2:c.1134A>T	XP_016870773.1:p.Pro378=
XR_001746415.2:n.2458A>T
XR_929874.3:n.2282A>T
NM_001190723.3:c.1842A>T	NP_001177652.1:p.Pro614=
NM_001005373.4:c.1923A>T MANE Select	NP_001005373.1:p.Pro641=
NM_001005374.4:c.1923A>T	NP_001005374.1:p.Pro641=
NM_001384142.1:c.1923A>T	NP_001371071.1:p.Pro641=
NM_001384143.1:c.1824A>T	NP_001371072.1:p.Pro608=
NM_001384144.1:c.1134A>T	NP_001371073.1:p.Pro378=
NR_168891.1:n.2452A>T
NR_168892.1:n.2276A>T