Canonical Allele Identifier: CA352913840

Gene: GNAT1

Linked Data

• MyVariant Identifiers: chr3:g.50230811A>T (hg19) ; chr3:g.50193378A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193378A>T , CM000665.2:g.50193378A>T	GRCh38
NC_000003.11:g.50230811A>T , CM000665.1:g.50230811A>T	GRCh37
NC_000003.10:g.50205815A>T	NCBI36
NG_009831.1:g.6769A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.263A>T MANE Select	ENSP00000232461.3:p.Asn88Ile
ENST00000232461.7:c.263A>T	ENSP00000232461.3:p.Asn88Ile
ENST00000433068.5:c.263A>T	ENSP00000387555.1:p.Asn88Ile
ENST00000440836.1:c.119A>T	ENSP00000403537.1:p.Asn40Ile
NM_000172.3:c.263A>T	NP_000163.2:p.Asn88Ile
NM_144499.2:c.263A>T	NP_653082.1:p.Asn88Ile
XM_011533595.1:c.119A>T	XP_011531897.1:p.Asn40Ile
XM_011533596.1:c.119A>T	XP_011531898.1:p.Asn40Ile
XR_940416.1:n.543A>T
NM_000172.4:c.263A>T	NP_000163.2:p.Asn88Ile
NM_144499.3:c.263A>T MANE Select	NP_653082.1:p.Asn88Ile