Canonical Allele Identifier: CA918936314

Gene: TYR

Linked Data

• dbSNP Id: rs1590902757

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285144del , CM000673.2:g.89285144del	GRCh38
NC_000011.9:g.89018312del , CM000673.1:g.89018312del	GRCh37
NC_000011.8:g.88657960del	NCBI36
NG_008748.1:g.112273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+190del MANE Select	ENSP00000263321.4:n.1366+190del
ENST00000263321.5:c.1366+190del	ENSP00000263321.4:n.1366+190del
ENST00000528243.1:n.364+190del
NM_000372.4:c.1366+190del	NP_000363.1:n.1366+190del
XM_011542970.1:c.1366+190del	XP_011541272.1:n.1366+190del
XM_011542970.2:c.1366+190del	XP_011541272.1:n.1366+190del
XR_001748321.1:n.2456+891del
XR_001748322.1:n.2457+891del
NM_000372.5:c.1366+190del MANE Select	NP_000363.1:n.1366+190del