Canonical Allele Identifier: CA2695215152

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178399_89178400del , CM000673.2:g.89178399_89178400del	GRCh38
NC_000011.9:g.88911567_88911568del , CM000673.1:g.88911567_88911568del	GRCh37
NC_000011.8:g.88551215_88551216del	NCBI36
NG_008748.1:g.5528_5529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.446_447del MANE Select	ENSP00000263321.4:p.Tyr149CysfsTer19
ENST00000263321.5:c.446_447del	ENSP00000263321.4:p.Tyr149CysfsTer19
ENST00000526139.1:n.507_508del
NM_000372.4:c.446_447del	NP_000363.1:p.Tyr149CysfsTer19
XM_011542970.1:c.446_447del	XP_011541272.1:p.Tyr149CysfsTer19
XM_011542970.2:c.446_447del	XP_011541272.1:p.Tyr149CysfsTer19
XR_001748321.1:n.2718-64866_2718-64865del
XR_001748322.1:n.2733-64866_2733-64865del
NM_000372.5:c.446_447del MANE Select	NP_000363.1:p.Tyr149CysfsTer19