Canonical Allele Identifier: CA1097665421

Gene: GNA12

Linked Data

• dbSNP Id: rs1793576937
• gnomAD v3: 7-2830369-CCTT-C
• gnomAD v4: 7-2830369-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2830372_2830374del , CM000669.2:g.2830372_2830374del	GRCh38
NC_000007.13:g.2870006_2870008del , CM000669.1:g.2870006_2870008del	GRCh37
NC_000007.12:g.2836532_2836534del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275364.8:c.309+13481_309+13483del MANE Select	ENSP00000275364.3:n.309+13481_309+13483de...
ENST00000275364.7:c.309+13481_309+13483del	ENSP00000275364.3:n.309+13481_309+13483de...
NM_001293092.1:c.309+13481_309+13483del	NP_001280021.1:n.309+13481_309+13483del
NM_007353.2:c.309+13481_309+13483del	NP_031379.2:n.309+13481_309+13483del
XM_011515288.1:c.19-35229_19-35227del	XP_011513590.1:n.19-35229_19-35227del
XM_011515288.3:c.19-35229_19-35227del	XP_011513590.1:n.19-35229_19-35227del
NM_007353.3:c.309+13481_309+13483del MANE Select	NP_031379.2:n.309+13481_309+13483del
NM_001293092.2:c.309+13481_309+13483del	NP_001280021.1:n.309+13481_309+13483del