Canonical Allele Identifier: CA1879828482

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501022_127501023delinsCA , CM000671.2:g.127501022_127501023delinsCA	GRCh38
NC_000009.11:g.130263301_130263302delinsCA , CM000671.1:g.130263301_130263302delinsCA	GRCh37
NC_000009.10:g.129303122_129303123delinsCA	NCBI36
NG_032008.1:g.54537_54538delinsCA , LRG_373:g.54537_54538delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1925_1926delinsCA MANE Select	ENSP00000300417.6:p.Pro642=
ENST00000472068.2:c.*1649_*1650delinsCA	ENSP00000501555.1:n.*1649_*1650delinsCA
ENST00000483302.6:n.2590_2591delinsCA
ENST00000498513.6:c.*816_*817delinsCA	ENSP00000501637.1:n.*816_*817delinsCA
ENST00000674511.1:n.1524_1525delinsCA
ENST00000674516.1:c.*541_*542delinsCA	ENSP00000502441.1:n.*541_*542delinsCA
ENST00000674621.1:n.1861-2351_1861-2350delinsCA
ENST00000674771.1:c.*568_*569delinsCA	ENSP00000502627.1:n.*568_*569delinsCA
ENST00000674784.1:c.*985_*986delinsCA	ENSP00000501837.1:n.*985_*986delinsCA
ENST00000674970.1:c.*1699_*1700delinsCA	ENSP00000502493.1:n.*1699_*1700delinsCA
ENST00000675012.1:n.1869_1870delinsCA
ENST00000675141.1:c.1826_1827delinsCA	ENSP00000502420.1:p.Pro609=
ENST00000675198.1:n.1805_1806delinsCA
ENST00000675213.1:c.1880_1881delinsCA	ENSP00000502218.1:p.Pro627=
ENST00000675224.1:c.1953_1954delinsCA	ENSP00000501869.1:p.Thr651=
ENST00000675253.1:c.*597_*598delinsCA	ENSP00000502557.1:n.*597_*598delinsCA
ENST00000675445.1:c.*1597_*1598delinsCA	ENSP00000502253.1:n.*1597_*1598delinsCA
ENST00000675448.1:c.1925_1926delinsCA	ENSP00000502167.1:p.Pro642=
ENST00000675521.1:n.1835_1836delinsCA
ENST00000675572.1:c.1826_1827delinsCA	ENSP00000501598.1:p.Pro609=
ENST00000675641.1:c.*667_*668delinsCA	ENSP00000501845.1:n.*667_*668delinsCA
ENST00000675657.1:c.*538_*539delinsCA	ENSP00000502002.1:n.*538_*539delinsCA
ENST00000675662.1:n.1720_1721delinsCA
ENST00000675789.1:c.1745_1746delinsCA	ENSP00000501954.1:p.Pro582=
ENST00000675883.1:c.1844_1845delinsCA	ENSP00000501592.1:p.Pro615=
ENST00000675945.1:c.*566_*567delinsCA	ENSP00000501835.1:n.*566_*567delinsCA
ENST00000676014.1:c.1868_1869delinsCA	ENSP00000502058.1:p.Pro623=
ENST00000676035.1:n.1587_1588delinsCA
ENST00000676106.1:n.1962_1963delinsCA
ENST00000676137.1:n.1955_1956delinsCA
ENST00000676170.1:c.2006_2007delinsCA	ENSP00000502177.1:p.Pro669=
ENST00000676318.1:c.*2755_*2756delinsCA	ENSP00000502300.1:n.*2755_*2756delinsCA
ENST00000676336.1:c.*538_*539delinsCA	ENSP00000502686.1:n.*538_*539delinsCA
ENST00000676349.1:c.*1613_*1614delinsCA	ENSP00000502155.1:n.*1613_*1614delinsCA
ENST00000676399.1:n.1828_1829delinsCA
ENST00000676409.1:n.1985_1986delinsCA
ENST00000300417.10:c.1925_1926delinsCA	ENSP00000300417.6:p.Pro642=
ENST00000323301.8:c.1925_1926delinsCA	ENSP00000322937.4:p.Pro642=
ENST00000373322.1:c.1925_1926delinsCA	ENSP00000362419.1:p.Pro642=
ENST00000373324.8:c.1844_1845delinsCA	ENSP00000362421.4:p.Pro615=
ENST00000472068.1:n.818_819delinsCA
ENST00000483302.5:n.1147_1148delinsCA
NM_001005373.3:c.1925_1926delinsCA	NP_001005373.1:p.Pro642=
NM_001005374.3:c.1925_1926delinsCA	NP_001005374.1:p.Pro642=
NM_001190723.2:c.1844_1845delinsCA	NP_001177652.1:p.Pro615=
NM_138361.5:c.1925_1926delinsCA , LRG_373t1:c.1925_1926delinsCA	NP_612370.3:p.Pro642=
XM_006717316.2:c.1826_1827delinsCA	XP_006717379.1:p.Pro609=
XM_006717316.4:c.1826_1827delinsCA	XP_006717379.1:p.Pro609=
XM_017015283.1:c.1925_1926delinsCA	XP_016870772.1:p.Pro642=
XM_017015284.2:c.1136_1137delinsCA	XP_016870773.1:p.Pro379=
XR_001746415.2:n.2460_2461delinsCA
XR_929874.3:n.2284_2285delinsCA
NM_001190723.3:c.1844_1845delinsCA	NP_001177652.1:p.Pro615=
NM_001005373.4:c.1925_1926delinsCA MANE Select	NP_001005373.1:p.Pro642=
NM_001005374.4:c.1925_1926delinsCA	NP_001005374.1:p.Pro642=
NM_001384142.1:c.1925_1926delinsCA	NP_001371071.1:p.Pro642=
NM_001384143.1:c.1826_1827delinsCA	NP_001371072.1:p.Pro609=
NM_001384144.1:c.1136_1137delinsCA	NP_001371073.1:p.Pro379=
NR_168891.1:n.2454_2455delinsCA
NR_168892.1:n.2278_2279delinsCA