Canonical Allele Identifier: CA2793087731

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178858_89178859insAGAG , CM000673.2:g.89178858_89178859insAGAG	GRCh38
NC_000011.9:g.88912026_88912027insAGAG , CM000673.1:g.88912026_88912027insAGAG	GRCh37
NC_000011.8:g.88551674_88551675insAGAG	NCBI36
NG_008748.1:g.5987_5988insAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+86_819+87insAGAG MANE Select	ENSP00000263321.4:n.819+86_819+87insAGAG
ENST00000263321.5:c.819+86_819+87insAGAG	ENSP00000263321.4:n.819+86_819+87insAGAG
ENST00000526139.1:n.880+86_880+87insAGAG
NM_000372.4:c.819+86_819+87insAGAG	NP_000363.1:n.819+86_819+87insAGAG
XM_011542970.1:c.819+86_819+87insAGAG	XP_011541272.1:n.819+86_819+87insAGAG
XM_011542970.2:c.819+86_819+87insAGAG	XP_011541272.1:n.819+86_819+87insAGAG
XR_001748321.1:n.2718-65326_2718-65325insCTCT
XR_001748322.1:n.2733-65326_2733-65325insCTCT
NM_000372.5:c.819+86_819+87insAGAG MANE Select	NP_000363.1:n.819+86_819+87insAGAG