Canonical Allele Identifier: CA433860438

Gene: GNAT1

Linked Data

• MyVariant Identifiers: chr3:g.50230749C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193316C>A , CM000665.2:g.50193316C>A	GRCh38
NC_000003.11:g.50230749C>A , CM000665.1:g.50230749C>A	GRCh37
NC_000003.10:g.50205753C>A	NCBI36
NG_009831.1:g.6707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.201C>A MANE Select	ENSP00000232461.3:p.Ala67=
ENST00000232461.7:c.201C>A	ENSP00000232461.3:p.Ala67=
ENST00000433068.5:c.201C>A	ENSP00000387555.1:p.Ala67=
ENST00000440836.1:c.57C>A	ENSP00000403537.1:p.Ala19=
NM_000172.3:c.201C>A	NP_000163.2:p.Ala67=
NM_144499.2:c.201C>A	NP_653082.1:p.Ala67=
XM_011533595.1:c.57C>A	XP_011531897.1:p.Ala19=
XM_011533596.1:c.57C>A	XP_011531898.1:p.Ala19=
XR_940416.1:n.481C>A
NM_000172.4:c.201C>A	NP_000163.2:p.Ala67=
NM_144499.3:c.201C>A MANE Select	NP_653082.1:p.Ala67=