Canonical Allele Identifier: CA6221369

Gene: TYR

Linked Data

• dbSNP Id: rs749756480
• ExAC: 11:89017898 TAC / T
• gnomAD v2: 11-89017898-TAC-T
• gnomAD v3: 11-89284730-TAC-T
• gnomAD v4: 11-89284730-TAC-T
• MyVariant Identifiers: chr11:g.89017899_89017900del (hg19) ; chr11:g.89284731_89284732del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284734_89284735del , CM000673.2:g.89284734_89284735del	GRCh38
NC_000011.9:g.89017902_89017903del , CM000673.1:g.89017902_89017903del	GRCh37
NC_000011.8:g.88657550_88657551del	NCBI36
NG_008748.1:g.111863_111864del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.1185-39_1185-38del MANE Select	ENSP00000263321.4:n.1185-39_1185-38del
ENST00000263321.5:c.1185-39_1185-38del	ENSP00000263321.4:n.1185-39_1185-38del
ENST00000528243.1:n.183-39_183-38del
NM_000372.4:c.1185-39_1185-38del	NP_000363.1:n.1185-39_1185-38del
XM_011542970.1:c.1185-39_1185-38del	XP_011541272.1:n.1185-39_1185-38del
XM_011542970.2:c.1185-39_1185-38del	XP_011541272.1:n.1185-39_1185-38del
XR_001748321.1:n.2456+1302_2456+1303del
XR_001748322.1:n.2457+1302_2457+1303del
NM_000372.5:c.1185-39_1185-38del MANE Select	NP_000363.1:n.1185-39_1185-38del