Canonical Allele Identifier: CA2412492

Gene: GNAT1

Linked Data

• dbSNP Id: rs746980027
• ExAC: 3:50230806 A / C
• gnomAD v2: 3-50230806-A-C
• MyVariant Identifiers: chr3:g.50230806A>C (hg19) ; chr3:g.50193373A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193373A>C , CM000665.2:g.50193373A>C	GRCh38
NC_000003.11:g.50230806A>C , CM000665.1:g.50230806A>C	GRCh37
NC_000003.10:g.50205810A>C	NCBI36
NG_009831.1:g.6764A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.258A>C MANE Select	ENSP00000232461.3:p.Thr86=
ENST00000232461.7:c.258A>C	ENSP00000232461.3:p.Thr86=
ENST00000433068.5:c.258A>C	ENSP00000387555.1:p.Thr86=
ENST00000440836.1:c.114A>C	ENSP00000403537.1:p.Thr38=
NM_000172.3:c.258A>C	NP_000163.2:p.Thr86=
NM_144499.2:c.258A>C	NP_653082.1:p.Thr86=
XM_011533595.1:c.114A>C	XP_011531897.1:p.Thr38=
XM_011533596.1:c.114A>C	XP_011531898.1:p.Thr38=
XR_940416.1:n.538A>C
NM_000172.4:c.258A>C	NP_000163.2:p.Thr86=
NM_144499.3:c.258A>C MANE Select	NP_653082.1:p.Thr86=