Canonical Allele Identifier: CA374938143

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263304T>A (hg19) ; chr9:g.127501025T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501025T>A , CM000671.2:g.127501025T>A	GRCh38
NC_000009.11:g.130263304T>A , CM000671.1:g.130263304T>A	GRCh37
NC_000009.10:g.129303125T>A	NCBI36
NG_032008.1:g.54540T>A , LRG_373:g.54540T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1928T>A MANE Select	ENSP00000300417.6:p.Met643Lys
ENST00000472068.2:c.*1652T>A	ENSP00000501555.1:n.*1652T>A
ENST00000483302.6:n.2593T>A
ENST00000498513.6:c.*819T>A	ENSP00000501637.1:n.*819T>A
ENST00000674511.1:n.1527T>A
ENST00000674516.1:c.*544T>A	ENSP00000502441.1:n.*544T>A
ENST00000674621.1:n.1861-2348T>A
ENST00000674771.1:c.*571T>A	ENSP00000502627.1:n.*571T>A
ENST00000674784.1:c.*988T>A	ENSP00000501837.1:n.*988T>A
ENST00000674970.1:c.*1702T>A	ENSP00000502493.1:n.*1702T>A
ENST00000675012.1:n.1872T>A
ENST00000675141.1:c.1829T>A	ENSP00000502420.1:p.Met610Lys
ENST00000675198.1:n.1808T>A
ENST00000675213.1:c.1883T>A	ENSP00000502218.1:p.Met628Lys
ENST00000675224.1:c.1956T>A	ENSP00000501869.1:p.Asn652Lys
ENST00000675253.1:c.*600T>A	ENSP00000502557.1:n.*600T>A
ENST00000675445.1:c.*1600T>A	ENSP00000502253.1:n.*1600T>A
ENST00000675448.1:c.1928T>A	ENSP00000502167.1:p.Met643Lys
ENST00000675521.1:n.1838T>A
ENST00000675572.1:c.1829T>A	ENSP00000501598.1:p.Met610Lys
ENST00000675641.1:c.*670T>A	ENSP00000501845.1:n.*670T>A
ENST00000675657.1:c.*541T>A	ENSP00000502002.1:n.*541T>A
ENST00000675662.1:n.1723T>A
ENST00000675789.1:c.1748T>A	ENSP00000501954.1:p.Met583Lys
ENST00000675883.1:c.1847T>A	ENSP00000501592.1:p.Met616Lys
ENST00000675945.1:c.*569T>A	ENSP00000501835.1:n.*569T>A
ENST00000676014.1:c.1871T>A	ENSP00000502058.1:p.Met624Lys
ENST00000676035.1:n.1590T>A
ENST00000676106.1:n.1965T>A
ENST00000676137.1:n.1958T>A
ENST00000676170.1:c.2009T>A	ENSP00000502177.1:p.Met670Lys
ENST00000676318.1:c.*2758T>A	ENSP00000502300.1:n.*2758T>A
ENST00000676336.1:c.*541T>A	ENSP00000502686.1:n.*541T>A
ENST00000676349.1:c.*1616T>A	ENSP00000502155.1:n.*1616T>A
ENST00000676399.1:n.1831T>A
ENST00000676409.1:n.1988T>A
ENST00000300417.10:c.1928T>A	ENSP00000300417.6:p.Met643Lys
ENST00000323301.8:c.1928T>A	ENSP00000322937.4:p.Met643Lys
ENST00000373322.1:c.1928T>A	ENSP00000362419.1:p.Met643Lys
ENST00000373324.8:c.1847T>A	ENSP00000362421.4:p.Met616Lys
ENST00000472068.1:n.821T>A
ENST00000483302.5:n.1150T>A
NM_001005373.3:c.1928T>A	NP_001005373.1:p.Met643Lys
NM_001005374.3:c.1928T>A	NP_001005374.1:p.Met643Lys
NM_001190723.2:c.1847T>A	NP_001177652.1:p.Met616Lys
NM_138361.5:c.1928T>A , LRG_373t1:c.1928T>A	NP_612370.3:p.Met643Lys
XM_006717316.2:c.1829T>A	XP_006717379.1:p.Met610Lys
XM_006717316.4:c.1829T>A	XP_006717379.1:p.Met610Lys
XM_017015283.1:c.1928T>A	XP_016870772.1:p.Met643Lys
XM_017015284.2:c.1139T>A	XP_016870773.1:p.Met380Lys
XR_001746415.2:n.2463T>A
XR_929874.3:n.2287T>A
NM_001190723.3:c.1847T>A	NP_001177652.1:p.Met616Lys
NM_001005373.4:c.1928T>A MANE Select	NP_001005373.1:p.Met643Lys
NM_001005374.4:c.1928T>A	NP_001005374.1:p.Met643Lys
NM_001384142.1:c.1928T>A	NP_001371071.1:p.Met643Lys
NM_001384143.1:c.1829T>A	NP_001371072.1:p.Met610Lys
NM_001384144.1:c.1139T>A	NP_001371073.1:p.Met380Lys
NR_168891.1:n.2457T>A
NR_168892.1:n.2281T>A