Canonical Allele Identifier: CA2793086059

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285031_89285034del , CM000673.2:g.89285031_89285034del	GRCh38
NC_000011.9:g.89018199_89018202del , CM000673.1:g.89018199_89018202del	GRCh37
NC_000011.8:g.88657847_88657850del	NCBI36
NG_008748.1:g.112160_112163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+77_1366+80del MANE Select	ENSP00000263321.4:n.1366+77_1366+80del
ENST00000263321.5:c.1366+77_1366+80del	ENSP00000263321.4:n.1366+77_1366+80del
ENST00000528243.1:n.364+77_364+80del
NM_000372.4:c.1366+77_1366+80del	NP_000363.1:n.1366+77_1366+80del
XM_011542970.1:c.1366+77_1366+80del	XP_011541272.1:n.1366+77_1366+80del
XM_011542970.2:c.1366+77_1366+80del	XP_011541272.1:n.1366+77_1366+80del
XR_001748321.1:n.2456+1001_2456+1004del
XR_001748322.1:n.2457+1001_2457+1004del
NM_000372.5:c.1366+77_1366+80del MANE Select	NP_000363.1:n.1366+77_1366+80del