Canonical Allele Identifier: CA1363836689

Gene: GNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193193_50193196delinsTCCC , CM000665.2:g.50193193_50193196delinsTCCC	GRCh38
NC_000003.11:g.50230626_50230629delinsTCCC , CM000665.1:g.50230626_50230629delinsTCCC	GRCh37
NC_000003.10:g.50205630_50205633delinsTCCC	NCBI36
NG_009831.1:g.6584_6587delinsTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.149+18_149+21delinsTCCC MANE Select	ENSP00000232461.3:n.149+18_149+21delinsTCCC
ENST00000232461.7:c.149+18_149+21delinsTCCC	ENSP00000232461.3:n.149+18_149+21delinsTCCC
ENST00000433068.5:c.149+18_149+21delinsTCCC	ENSP00000387555.1:n.149+18_149+21delinsTCCC
ENST00000440836.1:c.5+18_5+21delinsTCCC	ENSP00000403537.1:n.5+18_5+21delinsTCCC
NM_000172.3:c.149+18_149+21delinsTCCC	NP_000163.2:n.149+18_149+21delinsTCCC
NM_144499.2:c.149+18_149+21delinsTCCC	NP_653082.1:n.149+18_149+21delinsTCCC
XM_011533595.1:c.5+18_5+21delinsTCCC	XP_011531897.1:n.5+18_5+21delinsTCCC
XM_011533596.1:c.5+18_5+21delinsTCCC	XP_011531898.1:n.5+18_5+21delinsTCCC
XR_940416.1:n.429+18_429+21delinsTCCC
NM_000172.4:c.149+18_149+21delinsTCCC	NP_000163.2:n.149+18_149+21delinsTCCC
NM_144499.3:c.149+18_149+21delinsTCCC MANE Select	NP_653082.1:n.149+18_149+21delinsTCCC