Canonical Allele Identifier: CA2793086075

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285050_89285051insC , CM000673.2:g.89285050_89285051insC	GRCh38
NC_000011.9:g.89018218_89018219insC , CM000673.1:g.89018218_89018219insC	GRCh37
NC_000011.8:g.88657866_88657867insC	NCBI36
NG_008748.1:g.112179_112180insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+96_1366+97insC MANE Select	ENSP00000263321.4:n.1366+96_1366+97insC
ENST00000263321.5:c.1366+96_1366+97insC	ENSP00000263321.4:n.1366+96_1366+97insC
ENST00000528243.1:n.364+96_364+97insC
NM_000372.4:c.1366+96_1366+97insC	NP_000363.1:n.1366+96_1366+97insC
XM_011542970.1:c.1366+96_1366+97insC	XP_011541272.1:n.1366+96_1366+97insC
XM_011542970.2:c.1366+96_1366+97insC	XP_011541272.1:n.1366+96_1366+97insC
XR_001748321.1:n.2456+983_2456+984insG
XR_001748322.1:n.2457+983_2457+984insG
NM_000372.5:c.1366+96_1366+97insC MANE Select	NP_000363.1:n.1366+96_1366+97insC