Canonical Allele Identifier: CA374938317

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263393T>A (hg19) ; chr9:g.127501114T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501114T>A , CM000671.2:g.127501114T>A	GRCh38
NC_000009.11:g.130263393T>A , CM000671.1:g.130263393T>A	GRCh37
NC_000009.10:g.129303214T>A	NCBI36
NG_032008.1:g.54629T>A , LRG_373:g.54629T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2017T>A MANE Select	ENSP00000300417.6:p.Ser673Thr
ENST00000472068.2:c.*1741T>A	ENSP00000501555.1:n.*1741T>A
ENST00000483302.6:n.2682T>A
ENST00000498513.6:c.*908T>A	ENSP00000501637.1:n.*908T>A
ENST00000674511.1:n.1616T>A
ENST00000674516.1:c.*633T>A	ENSP00000502441.1:n.*633T>A
ENST00000674621.1:n.1861-2259T>A
ENST00000674771.1:c.*660T>A	ENSP00000502627.1:n.*660T>A
ENST00000674784.1:c.*1077T>A	ENSP00000501837.1:n.*1077T>A
ENST00000674970.1:c.*1791T>A	ENSP00000502493.1:n.*1791T>A
ENST00000675012.1:n.1961T>A
ENST00000675141.1:c.1918T>A	ENSP00000502420.1:p.Ser640Thr
ENST00000675198.1:n.1897T>A
ENST00000675213.1:c.1972T>A	ENSP00000502218.1:p.Ser658Thr
ENST00000675224.1:c.*83T>A	ENSP00000501869.1:n.*83T>A
ENST00000675253.1:c.*689T>A	ENSP00000502557.1:n.*689T>A
ENST00000675445.1:c.*1689T>A	ENSP00000502253.1:n.*1689T>A
ENST00000675448.1:c.2017T>A	ENSP00000502167.1:p.Ser673Thr
ENST00000675521.1:n.1927T>A
ENST00000675572.1:c.1918T>A	ENSP00000501598.1:p.Ser640Thr
ENST00000675641.1:c.*759T>A	ENSP00000501845.1:n.*759T>A
ENST00000675657.1:c.*630T>A	ENSP00000502002.1:n.*630T>A
ENST00000675662.1:n.1812T>A
ENST00000675789.1:c.1837T>A	ENSP00000501954.1:p.Ser613Thr
ENST00000675883.1:c.1936T>A	ENSP00000501592.1:p.Ser646Thr
ENST00000675945.1:c.*658T>A	ENSP00000501835.1:n.*658T>A
ENST00000676014.1:c.1960T>A	ENSP00000502058.1:p.Ser654Thr
ENST00000676035.1:n.1679T>A
ENST00000676106.1:n.2054T>A
ENST00000676137.1:n.2047T>A
ENST00000676170.1:c.2098T>A	ENSP00000502177.1:p.Ser700Thr
ENST00000676318.1:c.*2847T>A	ENSP00000502300.1:n.*2847T>A
ENST00000676336.1:c.*630T>A	ENSP00000502686.1:n.*630T>A
ENST00000676349.1:c.*1705T>A	ENSP00000502155.1:n.*1705T>A
ENST00000676399.1:n.1920T>A
ENST00000676409.1:n.2077T>A
ENST00000300417.10:c.2017T>A	ENSP00000300417.6:p.Ser673Thr
ENST00000323301.8:c.2017T>A	ENSP00000322937.4:p.Ser673Thr
ENST00000373322.1:c.2017T>A	ENSP00000362419.1:p.Ser673Thr
ENST00000373324.8:c.1936T>A	ENSP00000362421.4:p.Ser646Thr
ENST00000483302.5:n.1239T>A
NM_001005373.3:c.2017T>A	NP_001005373.1:p.Ser673Thr
NM_001005374.3:c.2017T>A	NP_001005374.1:p.Ser673Thr
NM_001190723.2:c.1936T>A	NP_001177652.1:p.Ser646Thr
NM_138361.5:c.2017T>A , LRG_373t1:c.2017T>A	NP_612370.3:p.Ser673Thr
XM_006717316.2:c.1918T>A	XP_006717379.1:p.Ser640Thr
XM_006717316.4:c.1918T>A	XP_006717379.1:p.Ser640Thr
XM_017015283.1:c.2017T>A	XP_016870772.1:p.Ser673Thr
XM_017015284.2:c.1228T>A	XP_016870773.1:p.Ser410Thr
XR_001746415.2:n.2552T>A
XR_929874.3:n.2376T>A
NM_001190723.3:c.1936T>A	NP_001177652.1:p.Ser646Thr
NM_001005373.4:c.2017T>A MANE Select	NP_001005373.1:p.Ser673Thr
NM_001005374.4:c.2017T>A	NP_001005374.1:p.Ser673Thr
NM_001384142.1:c.2017T>A	NP_001371071.1:p.Ser673Thr
NM_001384143.1:c.1918T>A	NP_001371072.1:p.Ser640Thr
NM_001384144.1:c.1228T>A	NP_001371073.1:p.Ser410Thr
NR_168891.1:n.2546T>A
NR_168892.1:n.2370T>A