Canonical Allele Identifier: CA2793087722

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178853_89178855del , CM000673.2:g.89178853_89178855del	GRCh38
NC_000011.9:g.88912021_88912023del , CM000673.1:g.88912021_88912023del	GRCh37
NC_000011.8:g.88551669_88551671del	NCBI36
NG_008748.1:g.5982_5984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+81_819+83del MANE Select	ENSP00000263321.4:n.819+81_819+83del
ENST00000263321.5:c.819+81_819+83del	ENSP00000263321.4:n.819+81_819+83del
ENST00000526139.1:n.880+81_880+83del
NM_000372.4:c.819+81_819+83del	NP_000363.1:n.819+81_819+83del
XM_011542970.1:c.819+81_819+83del	XP_011541272.1:n.819+81_819+83del
XM_011542970.2:c.819+81_819+83del	XP_011541272.1:n.819+81_819+83del
XR_001748321.1:n.2718-65322_2718-65320del
XR_001748322.1:n.2733-65322_2733-65320del
NM_000372.5:c.819+81_819+83del MANE Select	NP_000363.1:n.819+81_819+83del