Canonical Allele Identifier: CA1777428101
Gene: LSM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38173827A>C , CM000670.2:g.38173827A>C GRCh38
NC_000008.10:g.38031345A>C , CM000670.1:g.38031345A>C GRCh37
NC_000008.9:g.38150502A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000311351.9:c.47-1794T>G MANE Select ENSP00000310596.4:n.47-1794T>G
ENST00000311351.8:c.47-1794T>G ENSP00000310596.4:n.47-1794T>G
ENST00000520286.5:n.179-1794T>G
ENST00000520755.5:c.47-1794T>G ENSP00000430021.1:n.47-1794T>G
ENST00000522515.5:n.902-1794T>G
ENST00000523511.1:c.47-1794T>G ENSP00000428307.1:n.47-1794T>G
NM_014462.2:c.47-1794T>G NP_055277.1:n.47-1794T>G
NR_045492.1:n.457-1794T>G
NR_045493.1:n.179-1794T>G
NM_014462.3:c.47-1794T>G MANE Select NP_055277.1:n.47-1794T>G
NR_045492.2:n.220-1794T>G