Canonical Allele Identifier: CA2793087769

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178893_89178894insACA , CM000673.2:g.89178893_89178894insACA	GRCh38
NC_000011.9:g.88912061_88912062insACA , CM000673.1:g.88912061_88912062insACA	GRCh37
NC_000011.8:g.88551709_88551710insACA	NCBI36
NG_008748.1:g.6022_6023insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+121_819+122insACA MANE Select	ENSP00000263321.4:n.819+121_819+122insACA
ENST00000263321.5:c.819+121_819+122insACA	ENSP00000263321.4:n.819+121_819+122insACA
ENST00000526139.1:n.880+121_880+122insACA
NM_000372.4:c.819+121_819+122insACA	NP_000363.1:n.819+121_819+122insACA
XM_011542970.1:c.819+121_819+122insACA	XP_011541272.1:n.819+121_819+122insACA
XM_011542970.2:c.819+121_819+122insACA	XP_011541272.1:n.819+121_819+122insACA
XR_001748321.1:n.2718-65361_2718-65360insTGT
XR_001748322.1:n.2733-65361_2733-65360insTGT
NM_000372.5:c.819+121_819+122insACA MANE Select	NP_000363.1:n.819+121_819+122insACA