Canonical Allele Identifier: CA467236727

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263341T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501062T>C , CM000671.2:g.127501062T>C	GRCh38
NC_000009.11:g.130263341T>C , CM000671.1:g.130263341T>C	GRCh37
NC_000009.10:g.129303162T>C	NCBI36
NG_032008.1:g.54577T>C , LRG_373:g.54577T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1965T>C MANE Select	ENSP00000300417.6:p.Pro655=
ENST00000472068.2:c.*1689T>C	ENSP00000501555.1:n.*1689T>C
ENST00000483302.6:n.2630T>C
ENST00000498513.6:c.*856T>C	ENSP00000501637.1:n.*856T>C
ENST00000674511.1:n.1564T>C
ENST00000674516.1:c.*581T>C	ENSP00000502441.1:n.*581T>C
ENST00000674621.1:n.1861-2311T>C
ENST00000674771.1:c.*608T>C	ENSP00000502627.1:n.*608T>C
ENST00000674784.1:c.*1025T>C	ENSP00000501837.1:n.*1025T>C
ENST00000674970.1:c.*1739T>C	ENSP00000502493.1:n.*1739T>C
ENST00000675012.1:n.1909T>C
ENST00000675141.1:c.1866T>C	ENSP00000502420.1:p.Pro622=
ENST00000675198.1:n.1845T>C
ENST00000675213.1:c.1920T>C	ENSP00000502218.1:p.Pro640=
ENST00000675224.1:c.*31T>C	ENSP00000501869.1:n.*31T>C
ENST00000675253.1:c.*637T>C	ENSP00000502557.1:n.*637T>C
ENST00000675445.1:c.*1637T>C	ENSP00000502253.1:n.*1637T>C
ENST00000675448.1:c.1965T>C	ENSP00000502167.1:p.Pro655=
ENST00000675521.1:n.1875T>C
ENST00000675572.1:c.1866T>C	ENSP00000501598.1:p.Pro622=
ENST00000675641.1:c.*707T>C	ENSP00000501845.1:n.*707T>C
ENST00000675657.1:c.*578T>C	ENSP00000502002.1:n.*578T>C
ENST00000675662.1:n.1760T>C
ENST00000675789.1:c.1785T>C	ENSP00000501954.1:p.Pro595=
ENST00000675883.1:c.1884T>C	ENSP00000501592.1:p.Pro628=
ENST00000675945.1:c.*606T>C	ENSP00000501835.1:n.*606T>C
ENST00000676014.1:c.1908T>C	ENSP00000502058.1:p.Pro636=
ENST00000676035.1:n.1627T>C
ENST00000676106.1:n.2002T>C
ENST00000676137.1:n.1995T>C
ENST00000676170.1:c.2046T>C	ENSP00000502177.1:p.Pro682=
ENST00000676318.1:c.*2795T>C	ENSP00000502300.1:n.*2795T>C
ENST00000676336.1:c.*578T>C	ENSP00000502686.1:n.*578T>C
ENST00000676349.1:c.*1653T>C	ENSP00000502155.1:n.*1653T>C
ENST00000676399.1:n.1868T>C
ENST00000676409.1:n.2025T>C
ENST00000300417.10:c.1965T>C	ENSP00000300417.6:p.Pro655=
ENST00000323301.8:c.1965T>C	ENSP00000322937.4:p.Pro655=
ENST00000373322.1:c.1965T>C	ENSP00000362419.1:p.Pro655=
ENST00000373324.8:c.1884T>C	ENSP00000362421.4:p.Pro628=
ENST00000483302.5:n.1187T>C
NM_001005373.3:c.1965T>C	NP_001005373.1:p.Pro655=
NM_001005374.3:c.1965T>C	NP_001005374.1:p.Pro655=
NM_001190723.2:c.1884T>C	NP_001177652.1:p.Pro628=
NM_138361.5:c.1965T>C , LRG_373t1:c.1965T>C	NP_612370.3:p.Pro655=
XM_006717316.2:c.1866T>C	XP_006717379.1:p.Pro622=
XM_006717316.4:c.1866T>C	XP_006717379.1:p.Pro622=
XM_017015283.1:c.1965T>C	XP_016870772.1:p.Pro655=
XM_017015284.2:c.1176T>C	XP_016870773.1:p.Pro392=
XR_001746415.2:n.2500T>C
XR_929874.3:n.2324T>C
NM_001190723.3:c.1884T>C	NP_001177652.1:p.Pro628=
NM_001005373.4:c.1965T>C MANE Select	NP_001005373.1:p.Pro655=
NM_001005374.4:c.1965T>C	NP_001005374.1:p.Pro655=
NM_001384142.1:c.1965T>C	NP_001371071.1:p.Pro655=
NM_001384143.1:c.1866T>C	NP_001371072.1:p.Pro622=
NM_001384144.1:c.1176T>C	NP_001371073.1:p.Pro392=
NR_168891.1:n.2494T>C
NR_168892.1:n.2318T>C