Canonical Allele Identifier: CA467236621

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263302A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501023A>C , CM000671.2:g.127501023A>C	GRCh38
NC_000009.11:g.130263302A>C , CM000671.1:g.130263302A>C	GRCh37
NC_000009.10:g.129303123A>C	NCBI36
NG_032008.1:g.54538A>C , LRG_373:g.54538A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1926A>C MANE Select	ENSP00000300417.6:p.Pro642=
ENST00000472068.2:c.*1650A>C	ENSP00000501555.1:n.*1650A>C
ENST00000483302.6:n.2591A>C
ENST00000498513.6:c.*817A>C	ENSP00000501637.1:n.*817A>C
ENST00000674511.1:n.1525A>C
ENST00000674516.1:c.*542A>C	ENSP00000502441.1:n.*542A>C
ENST00000674621.1:n.1861-2350A>C
ENST00000674771.1:c.*569A>C	ENSP00000502627.1:n.*569A>C
ENST00000674784.1:c.*986A>C	ENSP00000501837.1:n.*986A>C
ENST00000674970.1:c.*1700A>C	ENSP00000502493.1:n.*1700A>C
ENST00000675012.1:n.1870A>C
ENST00000675141.1:c.1827A>C	ENSP00000502420.1:p.Pro609=
ENST00000675198.1:n.1806A>C
ENST00000675213.1:c.1881A>C	ENSP00000502218.1:p.Pro627=
ENST00000675224.1:c.1954A>C	ENSP00000501869.1:p.Asn652His
ENST00000675253.1:c.*598A>C	ENSP00000502557.1:n.*598A>C
ENST00000675445.1:c.*1598A>C	ENSP00000502253.1:n.*1598A>C
ENST00000675448.1:c.1926A>C	ENSP00000502167.1:p.Pro642=
ENST00000675521.1:n.1836A>C
ENST00000675572.1:c.1827A>C	ENSP00000501598.1:p.Pro609=
ENST00000675641.1:c.*668A>C	ENSP00000501845.1:n.*668A>C
ENST00000675657.1:c.*539A>C	ENSP00000502002.1:n.*539A>C
ENST00000675662.1:n.1721A>C
ENST00000675789.1:c.1746A>C	ENSP00000501954.1:p.Pro582=
ENST00000675883.1:c.1845A>C	ENSP00000501592.1:p.Pro615=
ENST00000675945.1:c.*567A>C	ENSP00000501835.1:n.*567A>C
ENST00000676014.1:c.1869A>C	ENSP00000502058.1:p.Pro623=
ENST00000676035.1:n.1588A>C
ENST00000676106.1:n.1963A>C
ENST00000676137.1:n.1956A>C
ENST00000676170.1:c.2007A>C	ENSP00000502177.1:p.Pro669=
ENST00000676318.1:c.*2756A>C	ENSP00000502300.1:n.*2756A>C
ENST00000676336.1:c.*539A>C	ENSP00000502686.1:n.*539A>C
ENST00000676349.1:c.*1614A>C	ENSP00000502155.1:n.*1614A>C
ENST00000676399.1:n.1829A>C
ENST00000676409.1:n.1986A>C
ENST00000300417.10:c.1926A>C	ENSP00000300417.6:p.Pro642=
ENST00000323301.8:c.1926A>C	ENSP00000322937.4:p.Pro642=
ENST00000373322.1:c.1926A>C	ENSP00000362419.1:p.Pro642=
ENST00000373324.8:c.1845A>C	ENSP00000362421.4:p.Pro615=
ENST00000472068.1:n.819A>C
ENST00000483302.5:n.1148A>C
NM_001005373.3:c.1926A>C	NP_001005373.1:p.Pro642=
NM_001005374.3:c.1926A>C	NP_001005374.1:p.Pro642=
NM_001190723.2:c.1845A>C	NP_001177652.1:p.Pro615=
NM_138361.5:c.1926A>C , LRG_373t1:c.1926A>C	NP_612370.3:p.Pro642=
XM_006717316.2:c.1827A>C	XP_006717379.1:p.Pro609=
XM_006717316.4:c.1827A>C	XP_006717379.1:p.Pro609=
XM_017015283.1:c.1926A>C	XP_016870772.1:p.Pro642=
XM_017015284.2:c.1137A>C	XP_016870773.1:p.Pro379=
XR_001746415.2:n.2461A>C
XR_929874.3:n.2285A>C
NM_001190723.3:c.1845A>C	NP_001177652.1:p.Pro615=
NM_001005373.4:c.1926A>C MANE Select	NP_001005373.1:p.Pro642=
NM_001005374.4:c.1926A>C	NP_001005374.1:p.Pro642=
NM_001384142.1:c.1926A>C	NP_001371071.1:p.Pro642=
NM_001384143.1:c.1827A>C	NP_001371072.1:p.Pro609=
NM_001384144.1:c.1137A>C	NP_001371073.1:p.Pro379=
NR_168891.1:n.2455A>C
NR_168892.1:n.2279A>C