Canonical Allele Identifier: CA1671216662
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795734_147795738delinsCCTGA , CM000668.2:g.147795734_147795738delinsCCTGA GRCh38
NC_000006.11:g.148116870_148116874delinsCCTGA , CM000668.1:g.148116870_148116874delinsCCTGA GRCh37
NC_000006.10:g.148158563_148158567delinsCCTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151738_460-151734delinsCCTGA XP_016866339.1:n.460-151738_460-151734delinsCCTGA