Canonical Allele Identifier: CA2665815002

Gene: GNAT1

Linked Data

• gnomAD v4: 3-50193233-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193233C>G , CM000665.2:g.50193233C>G	GRCh38
NC_000003.11:g.50230666C>G , CM000665.1:g.50230666C>G	GRCh37
NC_000003.10:g.50205670C>G	NCBI36
NG_009831.1:g.6624C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.150-32C>G MANE Select	ENSP00000232461.3:n.150-32C>G
ENST00000232461.7:c.150-32C>G	ENSP00000232461.3:n.150-32C>G
ENST00000433068.5:c.150-32C>G	ENSP00000387555.1:n.150-32C>G
ENST00000440836.1:c.6-32C>G	ENSP00000403537.1:n.6-32C>G
NM_000172.3:c.150-32C>G	NP_000163.2:n.150-32C>G
NM_144499.2:c.150-32C>G	NP_653082.1:n.150-32C>G
XM_011533595.1:c.6-32C>G	XP_011531897.1:n.6-32C>G
XM_011533596.1:c.6-32C>G	XP_011531898.1:n.6-32C>G
XR_940416.1:n.430-32C>G
NM_000172.4:c.150-32C>G	NP_000163.2:n.150-32C>G
NM_144499.3:c.150-32C>G MANE Select	NP_653082.1:n.150-32C>G