Canonical Allele Identifier: CA918936452

Gene: TYR

Linked Data

• dbSNP Id: rs1565386519

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178274_89178287del , CM000673.2:g.89178274_89178287del	GRCh38
NC_000011.9:g.88911442_88911455del , CM000673.1:g.88911442_88911455del	GRCh37
NC_000011.8:g.88551090_88551103del	NCBI36
NG_008748.1:g.5403_5416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.321_334del MANE Select	ENSP00000263321.4:p.Phe107LeufsTer?
ENST00000263321.5:c.321_334del	ENSP00000263321.4:p.Phe107LeufsTer?
ENST00000526139.1:n.382_395del
NM_000372.4:c.321_334del	NP_000363.1:p.Phe107LeufsTer?
XM_011542970.1:c.321_334del	XP_011541272.1:p.Phe107LeufsTer?
XM_011542970.2:c.321_334del	XP_011541272.1:p.Phe107LeufsTer?
XR_001748321.1:n.2718-64753_2718-64740del
XR_001748322.1:n.2733-64753_2733-64740del
NM_000372.5:c.321_334del MANE Select	NP_000363.1:p.Phe107LeufsTer?