Canonical Allele Identifier: CA2793086081

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285057_89285060del , CM000673.2:g.89285057_89285060del	GRCh38
NC_000011.9:g.89018225_89018228del , CM000673.1:g.89018225_89018228del	GRCh37
NC_000011.8:g.88657873_88657876del	NCBI36
NG_008748.1:g.112186_112189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+103_1366+106del MANE Select	ENSP00000263321.4:n.1366+103_1366+106del
ENST00000263321.5:c.1366+103_1366+106del	ENSP00000263321.4:n.1366+103_1366+106del
ENST00000528243.1:n.364+103_364+106del
NM_000372.4:c.1366+103_1366+106del	NP_000363.1:n.1366+103_1366+106del
XM_011542970.1:c.1366+103_1366+106del	XP_011541272.1:n.1366+103_1366+106del
XM_011542970.2:c.1366+103_1366+106del	XP_011541272.1:n.1366+103_1366+106del
XR_001748321.1:n.2456+974_2456+977del
XR_001748322.1:n.2457+974_2457+977del
NM_000372.5:c.1366+103_1366+106del MANE Select	NP_000363.1:n.1366+103_1366+106del