Canonical Allele Identifier: CA2756206785

Gene: GNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193436_50193437insACTT , CM000665.2:g.50193436_50193437insACTT	GRCh38
NC_000003.11:g.50230869_50230870insACTT , CM000665.1:g.50230869_50230870insACTT	GRCh37
NC_000003.10:g.50205873_50205874insACTT	NCBI36
NG_009831.1:g.6827_6828insACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.291+30_291+31insACTT MANE Select	ENSP00000232461.3:n.291+30_291+31insACTT
ENST00000232461.7:c.291+30_291+31insACTT	ENSP00000232461.3:n.291+30_291+31insACTT
ENST00000433068.5:c.291+30_291+31insACTT	ENSP00000387555.1:n.291+30_291+31insACTT
ENST00000440836.1:c.147+30_147+31insACTT	ENSP00000403537.1:n.147+30_147+31insACTT
NM_000172.3:c.291+30_291+31insACTT	NP_000163.2:n.291+30_291+31insACTT
NM_144499.2:c.291+30_291+31insACTT	NP_653082.1:n.291+30_291+31insACTT
XM_011533595.1:c.147+30_147+31insACTT	XP_011531897.1:n.147+30_147+31insACTT
XM_011533596.1:c.147+30_147+31insACTT	XP_011531898.1:n.147+30_147+31insACTT
XR_940416.1:n.571+30_571+31insACTT
NM_000172.4:c.291+30_291+31insACTT	NP_000163.2:n.291+30_291+31insACTT
NM_144499.3:c.291+30_291+31insACTT MANE Select	NP_653082.1:n.291+30_291+31insACTT