Canonical Allele Identifier: CA2580717029

Gene: GNA12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2830351T>G , CM000669.2:g.2830351T>G	GRCh38
NC_000007.13:g.2869985T>G , CM000669.1:g.2869985T>G	GRCh37
NC_000007.12:g.2836511T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275364.8:c.309+13502A>C MANE Select	ENSP00000275364.3:n.309+13502A>C
ENST00000275364.7:c.309+13502A>C	ENSP00000275364.3:n.309+13502A>C
NM_001293092.1:c.309+13502A>C	NP_001280021.1:n.309+13502A>C
NM_007353.2:c.309+13502A>C	NP_031379.2:n.309+13502A>C
XM_011515288.1:c.19-35208A>C	XP_011513590.1:n.19-35208A>C
XM_011515288.3:c.19-35208A>C	XP_011513590.1:n.19-35208A>C
NM_007353.3:c.309+13502A>C MANE Select	NP_031379.2:n.309+13502A>C
NM_001293092.2:c.309+13502A>C	NP_001280021.1:n.309+13502A>C