Canonical Allele Identifier: CA352894800

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293631A>T (hg19) ; chr3:g.50256199A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256199A>T , CM000665.2:g.50256199A>T	GRCh38
NC_000003.11:g.50293631A>T , CM000665.1:g.50293631A>T	GRCh37
NC_000003.10:g.50268635A>T	NCBI36
NG_016002.2:g.34512A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.472A>T MANE Select	ENSP00000312999.6:p.Asn158Tyr
ENST00000266027.9:c.316A>T	ENSP00000266027.6:p.Asn106Tyr
ENST00000313601.10:c.472A>T	ENSP00000312999.6:p.Asn158Tyr
ENST00000422163.5:c.424A>T	ENSP00000406871.1:p.Asn142Tyr
ENST00000440628.5:c.316A>T	ENSP00000395736.1:p.Asn106Tyr
ENST00000441156.5:c.429A>T	ENSP00000394321.1:p.Ter143Cys
ENST00000446079.5:c.*107A>T	ENSP00000406065.1:n.*107A>T
ENST00000451956.1:c.361A>T	ENSP00000406369.1:p.Asn121Tyr
ENST00000468422.1:n.39A>T
ENST00000490122.5:n.1299A>T
ENST00000491100.5:n.2288A>T
NM_001166425.1:c.361A>T	NP_001159897.1:p.Asn121Tyr
NM_001282617.1:c.316A>T	NP_001269546.1:p.Asn106Tyr
NM_001282618.1:c.229A>T	NP_001269547.1:p.Asn77Tyr
NM_001282619.1:c.424A>T	NP_001269548.1:p.Asn142Tyr
NM_001282620.1:c.424A>T	NP_001269549.1:p.Asn142Tyr
NM_002070.3:c.472A>T	NP_002061.1:p.Asn158Tyr
NM_002070.4:c.472A>T MANE Select	NP_002061.1:p.Asn158Tyr
NM_001166425.2:c.361A>T	NP_001159897.1:p.Asn121Tyr
NM_001282618.2:c.229A>T	NP_001269547.1:p.Asn77Tyr
NM_001282619.2:c.424A>T	NP_001269548.1:p.Asn142Tyr
NM_001282620.2:c.424A>T	NP_001269549.1:p.Asn142Tyr
NM_001282617.2:c.316A>T	NP_001269546.1:p.Asn106Tyr