Canonical Allele Identifier: CA2793087687

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178808_89178809insAGTT , CM000673.2:g.89178808_89178809insAGTT	GRCh38
NC_000011.9:g.88911976_88911977insAGTT , CM000673.1:g.88911976_88911977insAGTT	GRCh37
NC_000011.8:g.88551624_88551625insAGTT	NCBI36
NG_008748.1:g.5937_5938insAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+36_819+37insAGTT MANE Select	ENSP00000263321.4:n.819+36_819+37insAGTT
ENST00000263321.5:c.819+36_819+37insAGTT	ENSP00000263321.4:n.819+36_819+37insAGTT
ENST00000526139.1:n.880+36_880+37insAGTT
NM_000372.4:c.819+36_819+37insAGTT	NP_000363.1:n.819+36_819+37insAGTT
XM_011542970.1:c.819+36_819+37insAGTT	XP_011541272.1:n.819+36_819+37insAGTT
XM_011542970.2:c.819+36_819+37insAGTT	XP_011541272.1:n.819+36_819+37insAGTT
XR_001748321.1:n.2718-65276_2718-65275insAACT
XR_001748322.1:n.2733-65276_2733-65275insAACT
NM_000372.5:c.819+36_819+37insAGTT MANE Select	NP_000363.1:n.819+36_819+37insAGTT