Canonical Allele Identifier: CA2793087752

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178877_89178881del , CM000673.2:g.89178877_89178881del	GRCh38
NC_000011.9:g.88912045_88912049del , CM000673.1:g.88912045_88912049del	GRCh37
NC_000011.8:g.88551693_88551697del	NCBI36
NG_008748.1:g.6006_6010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+105_819+109del MANE Select	ENSP00000263321.4:n.819+105_819+109del
ENST00000263321.5:c.819+105_819+109del	ENSP00000263321.4:n.819+105_819+109del
ENST00000526139.1:n.880+105_880+109del
NM_000372.4:c.819+105_819+109del	NP_000363.1:n.819+105_819+109del
XM_011542970.1:c.819+105_819+109del	XP_011541272.1:n.819+105_819+109del
XM_011542970.2:c.819+105_819+109del	XP_011541272.1:n.819+105_819+109del
XR_001748321.1:n.2718-65348_2718-65344del
XR_001748322.1:n.2733-65348_2733-65344del
NM_000372.5:c.819+105_819+109del MANE Select	NP_000363.1:n.819+105_819+109del