Canonical Allele Identifier: CA2793087750

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178876_89178877insAG , CM000673.2:g.89178876_89178877insAG	GRCh38
NC_000011.9:g.88912044_88912045insAG , CM000673.1:g.88912044_88912045insAG	GRCh37
NC_000011.8:g.88551692_88551693insAG	NCBI36
NG_008748.1:g.6005_6006insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+104_819+105insAG MANE Select	ENSP00000263321.4:n.819+104_819+105insAG
ENST00000263321.5:c.819+104_819+105insAG	ENSP00000263321.4:n.819+104_819+105insAG
ENST00000526139.1:n.880+104_880+105insAG
NM_000372.4:c.819+104_819+105insAG	NP_000363.1:n.819+104_819+105insAG
XM_011542970.1:c.819+104_819+105insAG	XP_011541272.1:n.819+104_819+105insAG
XM_011542970.2:c.819+104_819+105insAG	XP_011541272.1:n.819+104_819+105insAG
XR_001748321.1:n.2718-65344_2718-65343insCT
XR_001748322.1:n.2733-65344_2733-65343insCT
NM_000372.5:c.819+104_819+105insAG MANE Select	NP_000363.1:n.819+104_819+105insAG