Canonical Allele Identifier: CA2793086066

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285037dup , CM000673.2:g.89285037dup	GRCh38
NC_000011.9:g.89018205dup , CM000673.1:g.89018205dup	GRCh37
NC_000011.8:g.88657853dup	NCBI36
NG_008748.1:g.112166dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+83dup MANE Select	ENSP00000263321.4:n.1366+83dup
ENST00000263321.5:c.1366+83dup	ENSP00000263321.4:n.1366+83dup
ENST00000528243.1:n.364+83dup
NM_000372.4:c.1366+83dup	NP_000363.1:n.1366+83dup
XM_011542970.1:c.1366+83dup	XP_011541272.1:n.1366+83dup
XM_011542970.2:c.1366+83dup	XP_011541272.1:n.1366+83dup
XR_001748321.1:n.2456+997dup
XR_001748322.1:n.2457+997dup
NM_000372.5:c.1366+83dup MANE Select	NP_000363.1:n.1366+83dup