Canonical Allele Identifier: CA2793087708

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178834_89178844del , CM000673.2:g.89178834_89178844del	GRCh38
NC_000011.9:g.88912002_88912012del , CM000673.1:g.88912002_88912012del	GRCh37
NC_000011.8:g.88551650_88551660del	NCBI36
NG_008748.1:g.5963_5973del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+62_819+72del MANE Select	ENSP00000263321.4:n.819+62_819+72del
ENST00000263321.5:c.819+62_819+72del	ENSP00000263321.4:n.819+62_819+72del
ENST00000526139.1:n.880+62_880+72del
NM_000372.4:c.819+62_819+72del	NP_000363.1:n.819+62_819+72del
XM_011542970.1:c.819+62_819+72del	XP_011541272.1:n.819+62_819+72del
XM_011542970.2:c.819+62_819+72del	XP_011541272.1:n.819+62_819+72del
XR_001748321.1:n.2718-65311_2718-65301del
XR_001748322.1:n.2733-65311_2733-65301del
NM_000372.5:c.819+62_819+72del MANE Select	NP_000363.1:n.819+62_819+72del