Canonical Allele Identifier: CA2793086062

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285032_89285033insACA , CM000673.2:g.89285032_89285033insACA	GRCh38
NC_000011.9:g.89018200_89018201insACA , CM000673.1:g.89018200_89018201insACA	GRCh37
NC_000011.8:g.88657848_88657849insACA	NCBI36
NG_008748.1:g.112161_112162insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+78_1366+79insACA MANE Select	ENSP00000263321.4:n.1366+78_1366+79insACA
ENST00000263321.5:c.1366+78_1366+79insACA	ENSP00000263321.4:n.1366+78_1366+79insACA
ENST00000528243.1:n.364+78_364+79insACA
NM_000372.4:c.1366+78_1366+79insACA	NP_000363.1:n.1366+78_1366+79insACA
XM_011542970.1:c.1366+78_1366+79insACA	XP_011541272.1:n.1366+78_1366+79insACA
XM_011542970.2:c.1366+78_1366+79insACA	XP_011541272.1:n.1366+78_1366+79insACA
XR_001748321.1:n.2456+1001_2456+1002insTGT
XR_001748322.1:n.2457+1001_2457+1002insTGT
NM_000372.5:c.1366+78_1366+79insACA MANE Select	NP_000363.1:n.1366+78_1366+79insACA