Canonical Allele Identifier: CA2793087765

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178890_89178891insACA , CM000673.2:g.89178890_89178891insACA	GRCh38
NC_000011.9:g.88912058_88912059insACA , CM000673.1:g.88912058_88912059insACA	GRCh37
NC_000011.8:g.88551706_88551707insACA	NCBI36
NG_008748.1:g.6019_6020insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+118_819+119insACA MANE Select	ENSP00000263321.4:n.819+118_819+119insACA
ENST00000263321.5:c.819+118_819+119insACA	ENSP00000263321.4:n.819+118_819+119insACA
ENST00000526139.1:n.880+118_880+119insACA
NM_000372.4:c.819+118_819+119insACA	NP_000363.1:n.819+118_819+119insACA
XM_011542970.1:c.819+118_819+119insACA	XP_011541272.1:n.819+118_819+119insACA
XM_011542970.2:c.819+118_819+119insACA	XP_011541272.1:n.819+118_819+119insACA
XR_001748321.1:n.2718-65358_2718-65357insTGT
XR_001748322.1:n.2733-65358_2733-65357insTGT
NM_000372.5:c.819+118_819+119insACA MANE Select	NP_000363.1:n.819+118_819+119insACA