Canonical Allele Identifier: CA2506340681

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127502770C>T , CM000671.2:g.127502770C>T	GRCh38
NC_000009.11:g.130265049C>T , CM000671.1:g.130265049C>T	GRCh37
NC_000009.10:g.129304870C>T	NCBI36
NG_032008.1:g.56285C>T , LRG_373:g.56285C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.2047-4C>T MANE Select	NP_001005373.1:n.2047-4C>T
ENST00000300417.11:c.2047-4C>T MANE Select	ENSP00000300417.6:n.2047-4C>T
NM_001005373.3:c.2047-4C>T	NP_001005373.1:n.2047-4C>T
NM_001005374.3:c.2047-4C>T	NP_001005374.1:n.2047-4C>T
NM_001005374.4:c.2047-4C>T	NP_001005374.1:n.2047-4C>T
NM_001190723.2:c.1966-4C>T	NP_001177652.1:n.1966-4C>T
NM_001190723.3:c.1966-4C>T	NP_001177652.1:n.1966-4C>T
NM_001384142.1:c.2047-4C>T	NP_001371071.1:n.2047-4C>T
NM_001384143.1:c.1948-4C>T	NP_001371072.1:n.1948-4C>T
NM_001384144.1:c.1258-4C>T	NP_001371073.1:n.1258-4C>T
NM_138361.5:c.2047-4C>T , LRG_373t1:c.2047-4C>T	NP_612370.3:n.2047-4C>T
NR_168891.1:n.2576-4C>T
NR_168892.1:n.2400-4C>T
ENST00000300417.10:c.2047-4C>T	ENSP00000300417.6:n.2047-4C>T
ENST00000323301.8:c.2047-4C>T	ENSP00000322937.4:n.2047-4C>T
ENST00000373322.1:c.2047-4C>T	ENSP00000362419.1:n.2047-4C>T
ENST00000373324.8:c.1966-4C>T	ENSP00000362421.4:n.1966-4C>T
ENST00000483302.5:n.1269-4C>T
ENST00000483302.6:n.2712-4C>T
ENST00000498513.6:c.*938-4C>T	ENSP00000501637.1:n.*938-4C>T
ENST00000674511.1:n.1646-4C>T
ENST00000674516.1:c.*663-4C>T	ENSP00000502441.1:n.*663-4C>T
ENST00000674621.1:n.1861-603C>T
ENST00000674771.1:c.*690-4C>T	ENSP00000502627.1:n.*690-4C>T
ENST00000674784.1:c.*1107-4C>T	ENSP00000501837.1:n.*1107-4C>T
ENST00000674970.1:c.*1821-4C>T	ENSP00000502493.1:n.*1821-4C>T
ENST00000675012.1:n.1991-4C>T
ENST00000675141.1:c.1948-4C>T	ENSP00000502420.1:n.1948-4C>T
ENST00000675198.1:n.1927-4C>T
ENST00000675213.1:c.2002-4C>T	ENSP00000502218.1:n.2002-4C>T
ENST00000675224.1:c.*113-4C>T	ENSP00000501869.1:n.*113-4C>T
ENST00000675253.1:c.*719-4C>T	ENSP00000502557.1:n.*719-4C>T
ENST00000675445.1:c.*1719-4C>T	ENSP00000502253.1:n.*1719-4C>T
ENST00000675448.1:c.2047-4C>T	ENSP00000502167.1:n.2047-4C>T
ENST00000675521.1:n.1957-4C>T
ENST00000675572.1:c.1948-4C>T	ENSP00000501598.1:n.1948-4C>T
ENST00000675641.1:c.*789-4C>T	ENSP00000501845.1:n.*789-4C>T
ENST00000675657.1:c.*660-4C>T	ENSP00000502002.1:n.*660-4C>T
ENST00000675662.1:n.1842-4C>T
ENST00000675789.1:c.1867-4C>T	ENSP00000501954.1:n.1867-4C>T
ENST00000675883.1:c.1966-4C>T	ENSP00000501592.1:n.1966-4C>T
ENST00000675945.1:c.*688-4C>T	ENSP00000501835.1:n.*688-4C>T
ENST00000676014.1:c.1990-4C>T	ENSP00000502058.1:n.1990-4C>T
ENST00000676035.1:n.1709-4C>T
ENST00000676106.1:n.2084-4C>T
ENST00000676137.1:n.2077-4C>T
ENST00000676170.1:c.2128-4C>T	ENSP00000502177.1:n.2128-4C>T
ENST00000676318.1:c.*2877-4C>T	ENSP00000502300.1:n.*2877-4C>T
ENST00000676336.1:c.*660-4C>T	ENSP00000502686.1:n.*660-4C>T
ENST00000676349.1:c.*1735-4C>T	ENSP00000502155.1:n.*1735-4C>T
ENST00000676399.1:n.1950-4C>T
ENST00000676409.1:n.2107-4C>T
XM_006717316.2:c.1948-4C>T	XP_006717379.1:n.1948-4C>T
XM_006717316.4:c.1948-4C>T	XP_006717379.1:n.1948-4C>T
XM_017015283.1:c.2047-4C>T	XP_016870772.1:n.2047-4C>T
XM_017015284.2:c.1258-4C>T	XP_016870773.1:n.1258-4C>T
XR_001746415.2:n.2582-4C>T
XR_929874.3:n.2406-4C>T