Canonical Allele Identifier: CA1989919650
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178213_89178216delinsGGAC , CM000673.2:g.89178213_89178216delinsGGAC GRCh38
NC_000011.9:g.88911381_88911384delinsGGAC , CM000673.1:g.88911381_88911384delinsGGAC GRCh37
NC_000011.8:g.88551029_88551032delinsGGAC NCBI36
NG_008748.1:g.5342_5345delinsGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.260_263delinsGGAC MANE Select ENSP00000263321.4:p.Arg87=
ENST00000263321.5:c.260_263delinsGGAC ENSP00000263321.4:p.Arg87=
ENST00000526139.1:n.321_324delinsGGAC
NM_000372.4:c.260_263delinsGGAC NP_000363.1:p.Arg87=
XM_011542970.1:c.260_263delinsGGAC XP_011541272.1:p.Arg87=
XM_011542970.2:c.260_263delinsGGAC XP_011541272.1:p.Arg87=
XR_001748321.1:n.2718-64683_2718-64680delinsGTCC
XR_001748322.1:n.2733-64683_2733-64680delinsGTCC
NM_000372.5:c.260_263delinsGGAC MANE Select NP_000363.1:p.Arg87=
Search 100 bp 5'
Search 100 bp 3'