Canonical Allele Identifier: CA433694617

Gene: GNAI2

Linked Data

• gnomAD v4: 3-50256198-G-T
• MyVariant Identifiers: chr3:g.50293630G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256198G>T , CM000665.2:g.50256198G>T	GRCh38
NC_000003.11:g.50293630G>T , CM000665.1:g.50293630G>T	GRCh37
NC_000003.10:g.50268634G>T	NCBI36
NG_016002.2:g.34511G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.471G>T MANE Select	ENSP00000312999.6:p.Leu157=
ENST00000266027.9:c.315G>T	ENSP00000266027.6:p.Leu105=
ENST00000313601.10:c.471G>T	ENSP00000312999.6:p.Leu157=
ENST00000422163.5:c.423G>T	ENSP00000406871.1:p.Leu141=
ENST00000440628.5:c.315G>T	ENSP00000395736.1:p.Leu105=
ENST00000441156.5:c.428G>T	ENSP00000394321.1:p.Ter143Leu
ENST00000446079.5:c.*106G>T	ENSP00000406065.1:n.*106G>T
ENST00000451956.1:c.360G>T	ENSP00000406369.1:p.Leu120=
ENST00000468422.1:n.38G>T
ENST00000490122.5:n.1298G>T
ENST00000491100.5:n.2287G>T
NM_001166425.1:c.360G>T	NP_001159897.1:p.Leu120=
NM_001282617.1:c.315G>T	NP_001269546.1:p.Leu105=
NM_001282618.1:c.228G>T	NP_001269547.1:p.Leu76=
NM_001282619.1:c.423G>T	NP_001269548.1:p.Leu141=
NM_001282620.1:c.423G>T	NP_001269549.1:p.Leu141=
NM_002070.3:c.471G>T	NP_002061.1:p.Leu157=
NM_002070.4:c.471G>T MANE Select	NP_002061.1:p.Leu157=
NM_001166425.2:c.360G>T	NP_001159897.1:p.Leu120=
NM_001282618.2:c.228G>T	NP_001269547.1:p.Leu76=
NM_001282619.2:c.423G>T	NP_001269548.1:p.Leu141=
NM_001282620.2:c.423G>T	NP_001269549.1:p.Leu141=
NM_001282617.2:c.315G>T	NP_001269546.1:p.Leu105=