Canonical Allele Identifier: CA2793086036

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285007_89285010del , CM000673.2:g.89285007_89285010del	GRCh38
NC_000011.9:g.89018175_89018178del , CM000673.1:g.89018175_89018178del	GRCh37
NC_000011.8:g.88657823_88657826del	NCBI36
NG_008748.1:g.112136_112139del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+53_1366+56del MANE Select	ENSP00000263321.4:n.1366+53_1366+56del
ENST00000263321.5:c.1366+53_1366+56del	ENSP00000263321.4:n.1366+53_1366+56del
ENST00000528243.1:n.364+53_364+56del
NM_000372.4:c.1366+53_1366+56del	NP_000363.1:n.1366+53_1366+56del
XM_011542970.1:c.1366+53_1366+56del	XP_011541272.1:n.1366+53_1366+56del
XM_011542970.2:c.1366+53_1366+56del	XP_011541272.1:n.1366+53_1366+56del
XR_001748321.1:n.2456+1024_2456+1027del
XR_001748322.1:n.2457+1024_2457+1027del
NM_000372.5:c.1366+53_1366+56del MANE Select	NP_000363.1:n.1366+53_1366+56del