Canonical Allele Identifier: CA2793087721

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178852_89178853insAGAG , CM000673.2:g.89178852_89178853insAGAG	GRCh38
NC_000011.9:g.88912020_88912021insAGAG , CM000673.1:g.88912020_88912021insAGAG	GRCh37
NC_000011.8:g.88551668_88551669insAGAG	NCBI36
NG_008748.1:g.5981_5982insAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+80_819+81insAGAG MANE Select	ENSP00000263321.4:n.819+80_819+81insAGAG
ENST00000263321.5:c.819+80_819+81insAGAG	ENSP00000263321.4:n.819+80_819+81insAGAG
ENST00000526139.1:n.880+80_880+81insAGAG
NM_000372.4:c.819+80_819+81insAGAG	NP_000363.1:n.819+80_819+81insAGAG
XM_011542970.1:c.819+80_819+81insAGAG	XP_011541272.1:n.819+80_819+81insAGAG
XM_011542970.2:c.819+80_819+81insAGAG	XP_011541272.1:n.819+80_819+81insAGAG
XR_001748321.1:n.2718-65320_2718-65319insCTCT
XR_001748322.1:n.2733-65320_2733-65319insCTCT
NM_000372.5:c.819+80_819+81insAGAG MANE Select	NP_000363.1:n.819+80_819+81insAGAG