Canonical Allele Identifier: CA2270641804

Gene: GNA13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65022415A= , CM000679.2:g.65022415A=	GRCh38
NC_000017.10:g.63018533A= , CM000679.1:g.63018533A=	GRCh37
NC_000017.9:g.60448995A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006572.6:c.511-4112T= MANE Select	NP_006563.2:n.511-4112T=
ENST00000439174.7:c.511-4112T= MANE Select	ENSP00000400717.2:n.511-4112T=
NM_001282425.1:c.226-4112T=	NP_001269354.1:n.226-4112T=
NM_001282425.2:c.226-4112T=	NP_001269354.1:n.226-4112T=
NM_006572.5:c.511-4112T=	NP_006563.2:n.511-4112T=
ENST00000439174.6:c.511-4112T=	ENSP00000400717.2:n.511-4112T=
ENST00000541118.1:c.226-4112T=	ENSP00000439647.1:n.226-4112T=
XM_011524202.1:c.511-4112T=	XP_011522504.1:n.511-4112T=
XR_934352.1:n.514-4112T=