Canonical Allele Identifier: CA2793087703

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178828_89178829insAC , CM000673.2:g.89178828_89178829insAC	GRCh38
NC_000011.9:g.88911996_88911997insAC , CM000673.1:g.88911996_88911997insAC	GRCh37
NC_000011.8:g.88551644_88551645insAC	NCBI36
NG_008748.1:g.5957_5958insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+56_819+57insAC MANE Select	ENSP00000263321.4:n.819+56_819+57insAC
ENST00000263321.5:c.819+56_819+57insAC	ENSP00000263321.4:n.819+56_819+57insAC
ENST00000526139.1:n.880+56_880+57insAC
NM_000372.4:c.819+56_819+57insAC	NP_000363.1:n.819+56_819+57insAC
XM_011542970.1:c.819+56_819+57insAC	XP_011541272.1:n.819+56_819+57insAC
XM_011542970.2:c.819+56_819+57insAC	XP_011541272.1:n.819+56_819+57insAC
XR_001748321.1:n.2718-65295_2718-65294insTG
XR_001748322.1:n.2733-65295_2733-65294insTG
NM_000372.5:c.819+56_819+57insAC MANE Select	NP_000363.1:n.819+56_819+57insAC