Canonical Allele Identifier: CA2793086103

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285098_89285099insAC , CM000673.2:g.89285098_89285099insAC	GRCh38
NC_000011.9:g.89018266_89018267insAC , CM000673.1:g.89018266_89018267insAC	GRCh37
NC_000011.8:g.88657914_88657915insAC	NCBI36
NG_008748.1:g.112227_112228insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+144_1366+145insAC MANE Select	ENSP00000263321.4:n.1366+144_1366+145insAC
ENST00000263321.5:c.1366+144_1366+145insAC	ENSP00000263321.4:n.1366+144_1366+145insAC
ENST00000528243.1:n.364+144_364+145insAC
NM_000372.4:c.1366+144_1366+145insAC	NP_000363.1:n.1366+144_1366+145insAC
XM_011542970.1:c.1366+144_1366+145insAC	XP_011541272.1:n.1366+144_1366+145insAC
XM_011542970.2:c.1366+144_1366+145insAC	XP_011541272.1:n.1366+144_1366+145insAC
XR_001748321.1:n.2456+935_2456+936insGT
XR_001748322.1:n.2457+935_2457+936insGT
NM_000372.5:c.1366+144_1366+145insAC MANE Select	NP_000363.1:n.1366+144_1366+145insAC