Canonical Allele Identifier: CA15891769

Gene: GNA13

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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