Canonical Allele Identifier: CA2793087795

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178931_89178934del , CM000673.2:g.89178931_89178934del	GRCh38
NC_000011.9:g.88912099_88912102del , CM000673.1:g.88912099_88912102del	GRCh37
NC_000011.8:g.88551747_88551750del	NCBI36
NG_008748.1:g.6060_6063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+159_819+162del MANE Select	ENSP00000263321.4:n.819+159_819+162del
ENST00000263321.5:c.819+159_819+162del	ENSP00000263321.4:n.819+159_819+162del
ENST00000526139.1:n.880+159_880+162del
NM_000372.4:c.819+159_819+162del	NP_000363.1:n.819+159_819+162del
XM_011542970.1:c.819+159_819+162del	XP_011541272.1:n.819+159_819+162del
XM_011542970.2:c.819+159_819+162del	XP_011541272.1:n.819+159_819+162del
XR_001748321.1:n.2718-65401_2718-65398del
XR_001748322.1:n.2733-65401_2733-65398del
NM_000372.5:c.819+159_819+162del MANE Select	NP_000363.1:n.819+159_819+162del