Canonical Allele Identifier: CA2615470674

Gene: TYR

Linked Data

• gnomAD v4: 11-89178851-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178852del , CM000673.2:g.89178852del	GRCh38
NC_000011.9:g.88912020del , CM000673.1:g.88912020del	GRCh37
NC_000011.8:g.88551668del	NCBI36
NG_008748.1:g.5981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+80del MANE Select	ENSP00000263321.4:n.819+80del
ENST00000263321.5:c.819+80del	ENSP00000263321.4:n.819+80del
ENST00000526139.1:n.880+80del
NM_000372.4:c.819+80del	NP_000363.1:n.819+80del
XM_011542970.1:c.819+80del	XP_011541272.1:n.819+80del
XM_011542970.2:c.819+80del	XP_011541272.1:n.819+80del
XR_001748321.1:n.2718-65319del
XR_001748322.1:n.2733-65319del
NM_000372.5:c.819+80del MANE Select	NP_000363.1:n.819+80del