Canonical Allele Identifier: CA2577808909

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256355A>T , CM000665.2:g.50256355A>T	GRCh38
NC_000003.11:g.50293787A>T , CM000665.1:g.50293787A>T	GRCh37
NC_000003.10:g.50268791A>T	NCBI36
NG_016002.2:g.34668A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.593+35A>T MANE Select	ENSP00000312999.6:n.593+35A>T
ENST00000266027.9:c.437+35A>T	ENSP00000266027.6:n.437+35A>T
ENST00000313601.10:c.593+35A>T	ENSP00000312999.6:n.593+35A>T
ENST00000422163.5:c.545+35A>T	ENSP00000406871.1:n.545+35A>T
ENST00000440628.5:c.437+35A>T	ENSP00000395736.1:n.437+35A>T
ENST00000441156.5:c.*121+35A>T	ENSP00000394321.1:n.*121+35A>T
ENST00000446079.5:c.*228+35A>T	ENSP00000406065.1:n.*228+35A>T
ENST00000451956.1:c.482+35A>T	ENSP00000406369.1:n.482+35A>T
ENST00000468422.1:n.195A>T
ENST00000490122.5:n.1420+35A>T
ENST00000491100.5:n.2409+35A>T
ENST00000492383.1:n.38+35A>T
NM_001166425.1:c.482+35A>T	NP_001159897.1:n.482+35A>T
NM_001282617.1:c.437+35A>T	NP_001269546.1:n.437+35A>T
NM_001282618.1:c.350+35A>T	NP_001269547.1:n.350+35A>T
NM_001282619.1:c.545+35A>T	NP_001269548.1:n.545+35A>T
NM_001282620.1:c.545+35A>T	NP_001269549.1:n.545+35A>T
NM_002070.3:c.593+35A>T	NP_002061.1:n.593+35A>T
NM_002070.4:c.593+35A>T MANE Select	NP_002061.1:n.593+35A>T
NM_001166425.2:c.482+35A>T	NP_001159897.1:n.482+35A>T
NM_001282618.2:c.350+35A>T	NP_001269547.1:n.350+35A>T
NM_001282619.2:c.545+35A>T	NP_001269548.1:n.545+35A>T
NM_001282620.2:c.545+35A>T	NP_001269549.1:n.545+35A>T
NM_001282617.2:c.437+35A>T	NP_001269546.1:n.437+35A>T