Canonical Allele Identifier: CA2793086101

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285090_89285091del , CM000673.2:g.89285090_89285091del	GRCh38
NC_000011.9:g.89018258_89018259del , CM000673.1:g.89018258_89018259del	GRCh37
NC_000011.8:g.88657906_88657907del	NCBI36
NG_008748.1:g.112219_112220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+136_1366+137del MANE Select	ENSP00000263321.4:n.1366+136_1366+137del
ENST00000263321.5:c.1366+136_1366+137del	ENSP00000263321.4:n.1366+136_1366+137del
ENST00000528243.1:n.364+136_364+137del
NM_000372.4:c.1366+136_1366+137del	NP_000363.1:n.1366+136_1366+137del
XM_011542970.1:c.1366+136_1366+137del	XP_011541272.1:n.1366+136_1366+137del
XM_011542970.2:c.1366+136_1366+137del	XP_011541272.1:n.1366+136_1366+137del
XR_001748321.1:n.2456+944_2456+945del
XR_001748322.1:n.2457+944_2457+945del
NM_000372.5:c.1366+136_1366+137del MANE Select	NP_000363.1:n.1366+136_1366+137del