Canonical Allele Identifier: CA3105361248

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50245358G>C , CM000665.2:g.50245358G>C	GRCh38
NC_000003.11:g.50282790G>C , CM000665.1:g.50282790G>C	GRCh37
NC_000003.10:g.50257794G>C	NCBI36
NG_016002.2:g.23671G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002070.4:c.119-6742G>C MANE Select	NP_002061.1:n.119-6742G>C
ENST00000313601.11:c.119-6742G>C MANE Select	ENSP00000312999.6:n.119-6742G>C
NM_001282617.1:c.-38-6742G>C	NP_001269546.1:n.-38-6742G>C
NM_001282617.2:c.-38-6742G>C	NP_001269546.1:n.-38-6742G>C
NM_001282618.1:c.-82-7039G>C	NP_001269547.1:n.-82-7039G>C
NM_001282618.2:c.-82-7039G>C	NP_001269547.1:n.-82-7039G>C
NM_001282619.1:c.-54-6262G>C	NP_001269548.1:n.-54-6262G>C
NM_001282619.2:c.-54-6262G>C	NP_001269548.1:n.-54-6262G>C
NM_001282620.1:c.71-6742G>C	NP_001269549.1:n.71-6742G>C
NM_001282620.2:c.71-6742G>C	NP_001269549.1:n.71-6742G>C
NM_002070.3:c.119-6742G>C	NP_002061.1:n.119-6742G>C
ENST00000266027.9:c.-38-6742G>C	ENSP00000266027.6:n.-38-6742G>C
ENST00000313601.10:c.119-6742G>C	ENSP00000312999.6:n.119-6742G>C
ENST00000422163.5:c.71-6742G>C	ENSP00000406871.1:n.71-6742G>C
ENST00000440628.5:c.-38-6742G>C	ENSP00000395736.1:n.-38-6742G>C
ENST00000441156.5:c.119-7039G>C	ENSP00000394321.1:n.119-7039G>C
ENST00000446079.5:c.71-6262G>C	ENSP00000406065.1:n.71-6262G>C
ENST00000491100.5:n.1935-6742G>C