Canonical Allele Identifier: CA1989921754

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178868_89178869delinsCA , CM000673.2:g.89178868_89178869delinsCA	GRCh38
NC_000011.9:g.88912036_88912037delinsCA , CM000673.1:g.88912036_88912037delinsCA	GRCh37
NC_000011.8:g.88551684_88551685delinsCA	NCBI36
NG_008748.1:g.5997_5998delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+96_819+97delinsCA MANE Select	ENSP00000263321.4:n.819+96_819+97delinsCA
ENST00000263321.5:c.819+96_819+97delinsCA	ENSP00000263321.4:n.819+96_819+97delinsCA
ENST00000526139.1:n.880+96_880+97delinsCA
NM_000372.4:c.819+96_819+97delinsCA	NP_000363.1:n.819+96_819+97delinsCA
XM_011542970.1:c.819+96_819+97delinsCA	XP_011541272.1:n.819+96_819+97delinsCA
XM_011542970.2:c.819+96_819+97delinsCA	XP_011541272.1:n.819+96_819+97delinsCA
XR_001748321.1:n.2718-65336_2718-65335delinsTG
XR_001748322.1:n.2733-65336_2733-65335delinsTG
NM_000372.5:c.819+96_819+97delinsCA MANE Select	NP_000363.1:n.819+96_819+97delinsCA