Canonical Allele Identifier: CA1989919913

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178288_89178290delinsGCA , CM000673.2:g.89178288_89178290delinsGCA	GRCh38
NC_000011.9:g.88911456_88911458delinsGCA , CM000673.1:g.88911456_88911458delinsGCA	GRCh37
NC_000011.8:g.88551104_88551106delinsGCA	NCBI36
NG_008748.1:g.5417_5419delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.335_337delinsGCA MANE Select	ENSP00000263321.4:p.Cys112=
ENST00000263321.5:c.335_337delinsGCA	ENSP00000263321.4:p.Cys112=
ENST00000526139.1:n.396_398delinsGCA
NM_000372.4:c.335_337delinsGCA	NP_000363.1:p.Cys112=
XM_011542970.1:c.335_337delinsGCA	XP_011541272.1:p.Cys112=
XM_011542970.2:c.335_337delinsGCA	XP_011541272.1:p.Cys112=
XR_001748321.1:n.2718-64757_2718-64755delinsTGC
XR_001748322.1:n.2733-64757_2733-64755delinsTGC
NM_000372.5:c.335_337delinsGCA MANE Select	NP_000363.1:p.Cys112=