Canonical Allele Identifier: CA2793086025

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284987_89284988insC , CM000673.2:g.89284987_89284988insC	GRCh38
NC_000011.9:g.89018155_89018156insC , CM000673.1:g.89018155_89018156insC	GRCh37
NC_000011.8:g.88657803_88657804insC	NCBI36
NG_008748.1:g.112116_112117insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+33_1366+34insC MANE Select	ENSP00000263321.4:n.1366+33_1366+34insC
ENST00000263321.5:c.1366+33_1366+34insC	ENSP00000263321.4:n.1366+33_1366+34insC
ENST00000528243.1:n.364+33_364+34insC
NM_000372.4:c.1366+33_1366+34insC	NP_000363.1:n.1366+33_1366+34insC
XM_011542970.1:c.1366+33_1366+34insC	XP_011541272.1:n.1366+33_1366+34insC
XM_011542970.2:c.1366+33_1366+34insC	XP_011541272.1:n.1366+33_1366+34insC
XR_001748321.1:n.2456+1046_2456+1047insG
XR_001748322.1:n.2457+1046_2457+1047insG
NM_000372.5:c.1366+33_1366+34insC MANE Select	NP_000363.1:n.1366+33_1366+34insC