Canonical Allele Identifier: CA940637735

Gene: TYR

Linked Data

• dbSNP Id: rs1943264675
• gnomAD v3: 11-89178868-CA-C
• gnomAD v4: 11-89178868-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178869del , CM000673.2:g.89178869del	GRCh38
NC_000011.9:g.88912037del , CM000673.1:g.88912037del	GRCh37
NC_000011.8:g.88551685del	NCBI36
NG_008748.1:g.5998del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+97del MANE Select	ENSP00000263321.4:n.819+97del
ENST00000263321.5:c.819+97del	ENSP00000263321.4:n.819+97del
ENST00000526139.1:n.880+97del
NM_000372.4:c.819+97del	NP_000363.1:n.819+97del
XM_011542970.1:c.819+97del	XP_011541272.1:n.819+97del
XM_011542970.2:c.819+97del	XP_011541272.1:n.819+97del
XR_001748321.1:n.2718-65336del
XR_001748322.1:n.2733-65336del
NM_000372.5:c.819+97del MANE Select	NP_000363.1:n.819+97del