Canonical Allele Identifier: CA352894804

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293632A>C (hg19) ; chr3:g.50256200A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256200A>C , CM000665.2:g.50256200A>C	GRCh38
NC_000003.11:g.50293632A>C , CM000665.1:g.50293632A>C	GRCh37
NC_000003.10:g.50268636A>C	NCBI36
NG_016002.2:g.34513A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.473A>C MANE Select	ENSP00000312999.6:p.Asn158Thr
ENST00000266027.9:c.317A>C	ENSP00000266027.6:p.Asn106Thr
ENST00000313601.10:c.473A>C	ENSP00000312999.6:p.Asn158Thr
ENST00000422163.5:c.425A>C	ENSP00000406871.1:p.Asn142Thr
ENST00000440628.5:c.317A>C	ENSP00000395736.1:p.Asn106Thr
ENST00000441156.5:c.*1A>C	ENSP00000394321.1:n.*1A>C
ENST00000446079.5:c.*108A>C	ENSP00000406065.1:n.*108A>C
ENST00000451956.1:c.362A>C	ENSP00000406369.1:p.Asn121Thr
ENST00000468422.1:n.40A>C
ENST00000490122.5:n.1300A>C
ENST00000491100.5:n.2289A>C
NM_001166425.1:c.362A>C	NP_001159897.1:p.Asn121Thr
NM_001282617.1:c.317A>C	NP_001269546.1:p.Asn106Thr
NM_001282618.1:c.230A>C	NP_001269547.1:p.Asn77Thr
NM_001282619.1:c.425A>C	NP_001269548.1:p.Asn142Thr
NM_001282620.1:c.425A>C	NP_001269549.1:p.Asn142Thr
NM_002070.3:c.473A>C	NP_002061.1:p.Asn158Thr
NM_002070.4:c.473A>C MANE Select	NP_002061.1:p.Asn158Thr
NM_001166425.2:c.362A>C	NP_001159897.1:p.Asn121Thr
NM_001282618.2:c.230A>C	NP_001269547.1:p.Asn77Thr
NM_001282619.2:c.425A>C	NP_001269548.1:p.Asn142Thr
NM_001282620.2:c.425A>C	NP_001269549.1:p.Asn142Thr
NM_001282617.2:c.317A>C	NP_001269546.1:p.Asn106Thr