Canonical Allele Identifier: CA1989921727

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178836_89178837delinsAG , CM000673.2:g.89178836_89178837delinsAG	GRCh38
NC_000011.9:g.88912004_88912005delinsAG , CM000673.1:g.88912004_88912005delinsAG	GRCh37
NC_000011.8:g.88551652_88551653delinsAG	NCBI36
NG_008748.1:g.5965_5966delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+64_819+65delinsAG MANE Select	ENSP00000263321.4:n.819+64_819+65delinsAG
ENST00000263321.5:c.819+64_819+65delinsAG	ENSP00000263321.4:n.819+64_819+65delinsAG
ENST00000526139.1:n.880+64_880+65delinsAG
NM_000372.4:c.819+64_819+65delinsAG	NP_000363.1:n.819+64_819+65delinsAG
XM_011542970.1:c.819+64_819+65delinsAG	XP_011541272.1:n.819+64_819+65delinsAG
XM_011542970.2:c.819+64_819+65delinsAG	XP_011541272.1:n.819+64_819+65delinsAG
XR_001748321.1:n.2718-65304_2718-65303delinsCT
XR_001748322.1:n.2733-65304_2733-65303delinsCT
NM_000372.5:c.819+64_819+65delinsAG MANE Select	NP_000363.1:n.819+64_819+65delinsAG