Canonical Allele Identifier: CA2793087716

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178841_89178842insAG , CM000673.2:g.89178841_89178842insAG	GRCh38
NC_000011.9:g.88912009_88912010insAG , CM000673.1:g.88912009_88912010insAG	GRCh37
NC_000011.8:g.88551657_88551658insAG	NCBI36
NG_008748.1:g.5970_5971insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+69_819+70insAG MANE Select	ENSP00000263321.4:n.819+69_819+70insAG
ENST00000263321.5:c.819+69_819+70insAG	ENSP00000263321.4:n.819+69_819+70insAG
ENST00000526139.1:n.880+69_880+70insAG
NM_000372.4:c.819+69_819+70insAG	NP_000363.1:n.819+69_819+70insAG
XM_011542970.1:c.819+69_819+70insAG	XP_011541272.1:n.819+69_819+70insAG
XM_011542970.2:c.819+69_819+70insAG	XP_011541272.1:n.819+69_819+70insAG
XR_001748321.1:n.2718-65309_2718-65308insCT
XR_001748322.1:n.2733-65309_2733-65308insCT
NM_000372.5:c.819+69_819+70insAG MANE Select	NP_000363.1:n.819+69_819+70insAG