Canonical Allele Identifier: CA401928299

Gene: GNAL

Linked Data

• MyVariant Identifiers: chr18:g.11881061A>G (hg19) ; chr18:g.11881062A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11881062A>G , CM000680.2:g.11881062A>G	GRCh38
NC_000018.9:g.11881061A>G , CM000680.1:g.11881061A>G	GRCh37
NC_000018.8:g.11871061A>G	NCBI36
NG_033866.1:g.197048A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334049.11:c.1304A>G MANE Select	ENSP00000334051.5:p.Asn435Ser
ENST00000423027.8:c.1073A>G MANE Plus Clinical	ENSP00000408489.2:p.Asn358Ser
ENST00000269162.9:c.1073A>G	ENSP00000269162.4:p.Asn358Ser
ENST00000334049.10:c.1304A>G	ENSP00000334051.5:p.Asn435Ser
ENST00000423027.7:c.1073A>G	ENSP00000408489.2:p.Asn358Ser
ENST00000535121.5:c.1073A>G	ENSP00000439023.1:p.Asn358Ser
ENST00000602628.1:c.452A>G	ENSP00000473600.1:p.Asn151Ser
NM_001142339.2:c.1073A>G	NP_001135811.1:p.Asn358Ser
NM_001261443.1:c.1073A>G	NP_001248372.1:p.Asn358Ser
NM_001261444.1:c.452A>G	NP_001248373.1:p.Asn151Ser
NM_182978.3:c.1304A>G	NP_892023.1:p.Asn435Ser
XM_006722323.2:c.1073A>G	XP_006722386.1:p.Asn358Ser
XM_011525654.1:c.1073A>G	XP_011523956.1:p.Asn358Ser
XM_024451164.1:c.1073A>G	XP_024306932.1:p.Asn358Ser
NM_182978.4:c.1304A>G MANE Select	NP_892023.1:p.Asn435Ser
NM_001261444.2:c.452A>G	NP_001248373.1:p.Asn151Ser
NM_001369387.1:c.1073A>G MANE Plus Clinical	NP_001356316.1:p.Asn358Ser
NM_001142339.3:c.1073A>G	NP_001135811.1:p.Asn358Ser
NM_001261443.2:c.1073A>G	NP_001248372.1:p.Asn358Ser