Canonical Allele Identifier: CA2793087775

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178897_89178898insACA , CM000673.2:g.89178897_89178898insACA	GRCh38
NC_000011.9:g.88912065_88912066insACA , CM000673.1:g.88912065_88912066insACA	GRCh37
NC_000011.8:g.88551713_88551714insACA	NCBI36
NG_008748.1:g.6026_6027insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+125_819+126insACA MANE Select	ENSP00000263321.4:n.819+125_819+126insACA
ENST00000263321.5:c.819+125_819+126insACA	ENSP00000263321.4:n.819+125_819+126insACA
ENST00000526139.1:n.880+125_880+126insACA
NM_000372.4:c.819+125_819+126insACA	NP_000363.1:n.819+125_819+126insACA
XM_011542970.1:c.819+125_819+126insACA	XP_011541272.1:n.819+125_819+126insACA
XM_011542970.2:c.819+125_819+126insACA	XP_011541272.1:n.819+125_819+126insACA
XR_001748321.1:n.2718-65365_2718-65364insTGT
XR_001748322.1:n.2733-65365_2733-65364insTGT
NM_000372.5:c.819+125_819+126insACA MANE Select	NP_000363.1:n.819+125_819+126insACA