Canonical Allele Identifier: CA2793086064

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285035_89285054del , CM000673.2:g.89285035_89285054del	GRCh38
NC_000011.9:g.89018203_89018222del , CM000673.1:g.89018203_89018222del	GRCh37
NC_000011.8:g.88657851_88657870del	NCBI36
NG_008748.1:g.112164_112183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+81_1366+100del MANE Select	ENSP00000263321.4:n.1366+81_1366+100del
ENST00000263321.5:c.1366+81_1366+100del	ENSP00000263321.4:n.1366+81_1366+100del
ENST00000528243.1:n.364+81_364+100del
NM_000372.4:c.1366+81_1366+100del	NP_000363.1:n.1366+81_1366+100del
XM_011542970.1:c.1366+81_1366+100del	XP_011541272.1:n.1366+81_1366+100del
XM_011542970.2:c.1366+81_1366+100del	XP_011541272.1:n.1366+81_1366+100del
XR_001748321.1:n.2456+980_2456+999del
XR_001748322.1:n.2457+980_2457+999del
NM_000372.5:c.1366+81_1366+100del MANE Select	NP_000363.1:n.1366+81_1366+100del