Canonical Allele Identifier: CA1683354004
Gene: GNA12 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2830378_2830380delinsTAA , CM000669.2:g.2830378_2830380delinsTAA GRCh38
NC_000007.13:g.2870012_2870014delinsTAA , CM000669.1:g.2870012_2870014delinsTAA GRCh37
NC_000007.12:g.2836538_2836540delinsTAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275364.8:c.309+13473_309+13475delinsTTA MANE Select ENSP00000275364.3:n.309+13473_309+13475de...
ENST00000275364.7:c.309+13473_309+13475delinsTTA ENSP00000275364.3:n.309+13473_309+13475de...
NM_001293092.1:c.309+13473_309+13475delinsTTA NP_001280021.1:n.309+13473_309+13475delin...
NM_007353.2:c.309+13473_309+13475delinsTTA NP_031379.2:n.309+13473_309+13475delinsTT...
XM_011515288.1:c.19-35237_19-35235delinsTTA XP_011513590.1:n.19-35237_19-35235delinsT...
XM_011515288.3:c.19-35237_19-35235delinsTTA XP_011513590.1:n.19-35237_19-35235delinsT...
NM_007353.3:c.309+13473_309+13475delinsTTA MANE Select NP_031379.2:n.309+13473_309+13475delinsTT...
NM_001293092.2:c.309+13473_309+13475delinsTTA NP_001280021.1:n.309+13473_309+13475delin...
Search 100 bp 5'
Search 100 bp 3'