Canonical Allele Identifier: CA1363836656

Gene: GNAT1

Linked Data

• dbSNP Id: rs1699439204
• gnomAD v3: 3-50193124-C-CAGA
• gnomAD v4: 3-50193124-C-CAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193124_50193125insAGA , CM000665.2:g.50193124_50193125insAGA	GRCh38
NC_000003.11:g.50230557_50230558insAGA , CM000665.1:g.50230557_50230558insAGA	GRCh37
NC_000003.10:g.50205561_50205562insAGA	NCBI36
NG_009831.1:g.6515_6516insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.107-9_107-8insAGA MANE Select	ENSP00000232461.3:n.107-9_107-8insAGA
ENST00000232461.7:c.107-9_107-8insAGA	ENSP00000232461.3:n.107-9_107-8insAGA
ENST00000433068.5:c.107-9_107-8insAGA	ENSP00000387555.1:n.107-9_107-8insAGA
ENST00000440836.1:c.-38-9_-38-8insAGA	ENSP00000403537.1:n.-38-9_-38-8insAGA
ENST00000467787.1:n.288-9_288-8insAGA
NM_000172.3:c.107-9_107-8insAGA	NP_000163.2:n.107-9_107-8insAGA
NM_144499.2:c.107-9_107-8insAGA	NP_653082.1:n.107-9_107-8insAGA
XM_011533595.1:c.-38-9_-38-8insAGA	XP_011531897.1:n.-38-9_-38-8insAGA
XM_011533596.1:c.-38-9_-38-8insAGA	XP_011531898.1:n.-38-9_-38-8insAGA
XR_940416.1:n.387-9_387-8insAGA
NM_000172.4:c.107-9_107-8insAGA	NP_000163.2:n.107-9_107-8insAGA
NM_144499.3:c.107-9_107-8insAGA MANE Select	NP_653082.1:n.107-9_107-8insAGA