Canonical Allele Identifier: CA1989921713

Gene: TYR

Linked Data

• dbSNP Id: rs1943264306

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178818_89178821del , CM000673.2:g.89178818_89178821del	GRCh38
NC_000011.9:g.88911986_88911989del , CM000673.1:g.88911986_88911989del	GRCh37
NC_000011.8:g.88551634_88551637del	NCBI36
NG_008748.1:g.5947_5950del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+46_819+49del MANE Select	ENSP00000263321.4:n.819+46_819+49del
ENST00000263321.5:c.819+46_819+49del	ENSP00000263321.4:n.819+46_819+49del
ENST00000526139.1:n.880+46_880+49del
NM_000372.4:c.819+46_819+49del	NP_000363.1:n.819+46_819+49del
XM_011542970.1:c.819+46_819+49del	XP_011541272.1:n.819+46_819+49del
XM_011542970.2:c.819+46_819+49del	XP_011541272.1:n.819+46_819+49del
XR_001748321.1:n.2718-65287_2718-65284del
XR_001748322.1:n.2733-65287_2733-65284del
NM_000372.5:c.819+46_819+49del MANE Select	NP_000363.1:n.819+46_819+49del