Canonical Allele Identifier: CA2793087754

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178878_89178882del , CM000673.2:g.89178878_89178882del	GRCh38
NC_000011.9:g.88912046_88912050del , CM000673.1:g.88912046_88912050del	GRCh37
NC_000011.8:g.88551694_88551698del	NCBI36
NG_008748.1:g.6007_6011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+106_819+110del MANE Select	ENSP00000263321.4:n.819+106_819+110del
ENST00000263321.5:c.819+106_819+110del	ENSP00000263321.4:n.819+106_819+110del
ENST00000526139.1:n.880+106_880+110del
NM_000372.4:c.819+106_819+110del	NP_000363.1:n.819+106_819+110del
XM_011542970.1:c.819+106_819+110del	XP_011541272.1:n.819+106_819+110del
XM_011542970.2:c.819+106_819+110del	XP_011541272.1:n.819+106_819+110del
XR_001748321.1:n.2718-65349_2718-65345del
XR_001748322.1:n.2733-65349_2733-65345del
NM_000372.5:c.819+106_819+110del MANE Select	NP_000363.1:n.819+106_819+110del