Canonical Allele Identifier: CA2793087718

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178851_89178980del , CM000673.2:g.89178851_89178980del	GRCh38
NC_000011.9:g.88912019_88912148del , CM000673.1:g.88912019_88912148del	GRCh37
NC_000011.8:g.88551667_88551796del	NCBI36
NG_008748.1:g.5980_6109del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+79_819+208del MANE Select	ENSP00000263321.4:n.819+79_819+208del
ENST00000263321.5:c.819+79_819+208del	ENSP00000263321.4:n.819+79_819+208del
ENST00000526139.1:n.880+79_880+208del
NM_000372.4:c.819+79_819+208del	NP_000363.1:n.819+79_819+208del
XM_011542970.1:c.819+79_819+208del	XP_011541272.1:n.819+79_819+208del
XM_011542970.2:c.819+79_819+208del	XP_011541272.1:n.819+79_819+208del
XR_001748321.1:n.2718-65441_2718-65312del
XR_001748322.1:n.2733-65441_2733-65312del
NM_000372.5:c.819+79_819+208del MANE Select	NP_000363.1:n.819+79_819+208del