Canonical Allele Identifier: CA2691763576

Gene: LRSAM1

Linked Data

• gnomAD v4: 9-127500916-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127500916C>T , CM000671.2:g.127500916C>T	GRCh38
NC_000009.11:g.130263195C>T , CM000671.1:g.130263195C>T	GRCh37
NC_000009.10:g.129303016C>T	NCBI36
NG_032008.1:g.54431C>T , LRG_373:g.54431C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1913-94C>T MANE Select	ENSP00000300417.6:n.1913-94C>T
ENST00000472068.2:c.*1637-94C>T	ENSP00000501555.1:n.*1637-94C>T
ENST00000483302.6:n.2578-94C>T
ENST00000498513.6:c.*804-94C>T	ENSP00000501637.1:n.*804-94C>T
ENST00000674511.1:n.1512-94C>T
ENST00000674516.1:c.*529-94C>T	ENSP00000502441.1:n.*529-94C>T
ENST00000674621.1:n.1861-2457C>T
ENST00000674771.1:c.*556-94C>T	ENSP00000502627.1:n.*556-94C>T
ENST00000674784.1:c.*973-94C>T	ENSP00000501837.1:n.*973-94C>T
ENST00000674970.1:c.*1687-94C>T	ENSP00000502493.1:n.*1687-94C>T
ENST00000675012.1:n.1857-94C>T
ENST00000675141.1:c.1814-94C>T	ENSP00000502420.1:n.1814-94C>T
ENST00000675198.1:n.1793-94C>T
ENST00000675213.1:c.1868-94C>T	ENSP00000502218.1:n.1868-94C>T
ENST00000675224.1:c.1941-94C>T	ENSP00000501869.1:n.1941-94C>T
ENST00000675253.1:c.*585-94C>T	ENSP00000502557.1:n.*585-94C>T
ENST00000675445.1:c.*1585-94C>T	ENSP00000502253.1:n.*1585-94C>T
ENST00000675448.1:c.1913-94C>T	ENSP00000502167.1:n.1913-94C>T
ENST00000675521.1:n.1823-94C>T
ENST00000675572.1:c.1814-94C>T	ENSP00000501598.1:n.1814-94C>T
ENST00000675641.1:c.*655-94C>T	ENSP00000501845.1:n.*655-94C>T
ENST00000675657.1:c.*526-94C>T	ENSP00000502002.1:n.*526-94C>T
ENST00000675662.1:n.1708-94C>T
ENST00000675789.1:c.1733-94C>T	ENSP00000501954.1:n.1733-94C>T
ENST00000675883.1:c.1832-94C>T	ENSP00000501592.1:n.1832-94C>T
ENST00000675945.1:c.*554-94C>T	ENSP00000501835.1:n.*554-94C>T
ENST00000676014.1:c.1856-94C>T	ENSP00000502058.1:n.1856-94C>T
ENST00000676035.1:n.1575-94C>T
ENST00000676106.1:n.1950-94C>T
ENST00000676137.1:n.1943-94C>T
ENST00000676170.1:c.1994-94C>T	ENSP00000502177.1:n.1994-94C>T
ENST00000676318.1:c.*2743-94C>T	ENSP00000502300.1:n.*2743-94C>T
ENST00000676336.1:c.*526-94C>T	ENSP00000502686.1:n.*526-94C>T
ENST00000676349.1:c.*1601-94C>T	ENSP00000502155.1:n.*1601-94C>T
ENST00000676399.1:n.1816-94C>T
ENST00000676409.1:n.1973-94C>T
ENST00000300417.10:c.1913-94C>T	ENSP00000300417.6:n.1913-94C>T
ENST00000323301.8:c.1913-94C>T	ENSP00000322937.4:n.1913-94C>T
ENST00000373322.1:c.1913-94C>T	ENSP00000362419.1:n.1913-94C>T
ENST00000373324.8:c.1832-94C>T	ENSP00000362421.4:n.1832-94C>T
ENST00000472068.1:n.806-94C>T
ENST00000483302.5:n.1135-94C>T
NM_001005373.3:c.1913-94C>T	NP_001005373.1:n.1913-94C>T
NM_001005374.3:c.1913-94C>T	NP_001005374.1:n.1913-94C>T
NM_001190723.2:c.1832-94C>T	NP_001177652.1:n.1832-94C>T
NM_138361.5:c.1913-94C>T , LRG_373t1:c.1913-94C>T	NP_612370.3:n.1913-94C>T
XM_006717316.2:c.1814-94C>T	XP_006717379.1:n.1814-94C>T
XM_006717316.4:c.1814-94C>T	XP_006717379.1:n.1814-94C>T
XM_017015283.1:c.1913-94C>T	XP_016870772.1:n.1913-94C>T
XM_017015284.2:c.1124-94C>T	XP_016870773.1:n.1124-94C>T
XR_001746415.2:n.2448-94C>T
XR_929874.3:n.2272-94C>T
NM_001190723.3:c.1832-94C>T	NP_001177652.1:n.1832-94C>T
NM_001005373.4:c.1913-94C>T MANE Select	NP_001005373.1:n.1913-94C>T
NM_001005374.4:c.1913-94C>T	NP_001005374.1:n.1913-94C>T
NM_001384142.1:c.1913-94C>T	NP_001371071.1:n.1913-94C>T
NM_001384143.1:c.1814-94C>T	NP_001371072.1:n.1814-94C>T
NM_001384144.1:c.1124-94C>T	NP_001371073.1:n.1124-94C>T
NR_168891.1:n.2442-94C>T
NR_168892.1:n.2266-94C>T