Canonical Allele Identifier: CA2793087759

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178885dup , CM000673.2:g.89178885dup	GRCh38
NC_000011.9:g.88912053dup , CM000673.1:g.88912053dup	GRCh37
NC_000011.8:g.88551701dup	NCBI36
NG_008748.1:g.6014dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+113dup MANE Select	ENSP00000263321.4:n.819+113dup
ENST00000263321.5:c.819+113dup	ENSP00000263321.4:n.819+113dup
ENST00000526139.1:n.880+113dup
NM_000372.4:c.819+113dup	NP_000363.1:n.819+113dup
XM_011542970.1:c.819+113dup	XP_011541272.1:n.819+113dup
XM_011542970.2:c.819+113dup	XP_011541272.1:n.819+113dup
XR_001748321.1:n.2718-65352dup
XR_001748322.1:n.2733-65352dup
NM_000372.5:c.819+113dup MANE Select	NP_000363.1:n.819+113dup