Canonical Allele Identifier: CA2793087714

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178839_89178840insACA , CM000673.2:g.89178839_89178840insACA	GRCh38
NC_000011.9:g.88912007_88912008insACA , CM000673.1:g.88912007_88912008insACA	GRCh37
NC_000011.8:g.88551655_88551656insACA	NCBI36
NG_008748.1:g.5968_5969insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+67_819+68insACA MANE Select	ENSP00000263321.4:n.819+67_819+68insACA
ENST00000263321.5:c.819+67_819+68insACA	ENSP00000263321.4:n.819+67_819+68insACA
ENST00000526139.1:n.880+67_880+68insACA
NM_000372.4:c.819+67_819+68insACA	NP_000363.1:n.819+67_819+68insACA
XM_011542970.1:c.819+67_819+68insACA	XP_011541272.1:n.819+67_819+68insACA
XM_011542970.2:c.819+67_819+68insACA	XP_011541272.1:n.819+67_819+68insACA
XR_001748321.1:n.2718-65307_2718-65306insTGT
XR_001748322.1:n.2733-65307_2733-65306insTGT
NM_000372.5:c.819+67_819+68insACA MANE Select	NP_000363.1:n.819+67_819+68insACA