Canonical Allele Identifier: CA2615470510

Gene: TYR

Linked Data

• gnomAD v4: 11-89178509-GATGCACTGCTTGGGGGATCTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178511_89178532del , CM000673.2:g.89178511_89178532del	GRCh38
NC_000011.9:g.88911679_88911700del , CM000673.1:g.88911679_88911700del	GRCh37
NC_000011.8:g.88551327_88551348del	NCBI36
NG_008748.1:g.5640_5661del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.558_579del MANE Select	ENSP00000263321.4:p.Asp186GlufsTer?
ENST00000263321.5:c.558_579del	ENSP00000263321.4:p.Asp186GlufsTer?
ENST00000526139.1:n.619_640del
NM_000372.4:c.558_579del	NP_000363.1:p.Asp186GlufsTer?
XM_011542970.1:c.558_579del	XP_011541272.1:p.Asp186GlufsTer?
XM_011542970.2:c.558_579del	XP_011541272.1:p.Asp186GlufsTer?
XR_001748321.1:n.2718-64998_2718-64977del
XR_001748322.1:n.2733-64998_2733-64977del
NM_000372.5:c.558_579del MANE Select	NP_000363.1:p.Asp186GlufsTer?