Canonical Allele Identifier: CA2793087740

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178871_89178875del , CM000673.2:g.89178871_89178875del	GRCh38
NC_000011.9:g.88912039_88912043del , CM000673.1:g.88912039_88912043del	GRCh37
NC_000011.8:g.88551687_88551691del	NCBI36
NG_008748.1:g.6000_6004del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+99_819+103del MANE Select	ENSP00000263321.4:n.819+99_819+103del
ENST00000263321.5:c.819+99_819+103del	ENSP00000263321.4:n.819+99_819+103del
ENST00000526139.1:n.880+99_880+103del
NM_000372.4:c.819+99_819+103del	NP_000363.1:n.819+99_819+103del
XM_011542970.1:c.819+99_819+103del	XP_011541272.1:n.819+99_819+103del
XM_011542970.2:c.819+99_819+103del	XP_011541272.1:n.819+99_819+103del
XR_001748321.1:n.2718-65342_2718-65338del
XR_001748322.1:n.2733-65342_2733-65338del
NM_000372.5:c.819+99_819+103del MANE Select	NP_000363.1:n.819+99_819+103del