Canonical Allele Identifier: CA1989972553

Gene: TYR

Linked Data

• dbSNP Id: rs1944768206
• gnomAD v4: 11-89285087-AATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285091_89285094del , CM000673.2:g.89285091_89285094del	GRCh38
NC_000011.9:g.89018259_89018262del , CM000673.1:g.89018259_89018262del	GRCh37
NC_000011.8:g.88657907_88657910del	NCBI36
NG_008748.1:g.112220_112223del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+137_1366+140del MANE Select	ENSP00000263321.4:n.1366+137_1366+140del
ENST00000263321.5:c.1366+137_1366+140del	ENSP00000263321.4:n.1366+137_1366+140del
ENST00000528243.1:n.364+137_364+140del
NM_000372.4:c.1366+137_1366+140del	NP_000363.1:n.1366+137_1366+140del
XM_011542970.1:c.1366+137_1366+140del	XP_011541272.1:n.1366+137_1366+140del
XM_011542970.2:c.1366+137_1366+140del	XP_011541272.1:n.1366+137_1366+140del
XR_001748321.1:n.2456+943_2456+946del
XR_001748322.1:n.2457+943_2457+946del
NM_000372.5:c.1366+137_1366+140del MANE Select	NP_000363.1:n.1366+137_1366+140del