Canonical Allele Identifier: CA1395448060
Gene: LSAMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117061134_117061135delinsTC , CM000665.2:g.117061134_117061135delinsTC GRCh38
NC_000003.11:g.116779981_116779982delinsTC , CM000665.1:g.116779981_116779982delinsTC GRCh37
NC_000003.10:g.118262671_118262672delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000474851.1:c.34-51761_34-51760delinsGA ENSP00000418506.1:n.34-51761_34-51760delinsGA