Canonical Allele Identifier: CA2793087692

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178811_89178812insG , CM000673.2:g.89178811_89178812insG	GRCh38
NC_000011.9:g.88911979_88911980insG , CM000673.1:g.88911979_88911980insG	GRCh37
NC_000011.8:g.88551627_88551628insG	NCBI36
NG_008748.1:g.5940_5941insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+39_819+40insG MANE Select	ENSP00000263321.4:n.819+39_819+40insG
ENST00000263321.5:c.819+39_819+40insG	ENSP00000263321.4:n.819+39_819+40insG
ENST00000526139.1:n.880+39_880+40insG
NM_000372.4:c.819+39_819+40insG	NP_000363.1:n.819+39_819+40insG
XM_011542970.1:c.819+39_819+40insG	XP_011541272.1:n.819+39_819+40insG
XM_011542970.2:c.819+39_819+40insG	XP_011541272.1:n.819+39_819+40insG
XR_001748321.1:n.2718-65279_2718-65278insC
XR_001748322.1:n.2733-65279_2733-65278insC
NM_000372.5:c.819+39_819+40insG MANE Select	NP_000363.1:n.819+39_819+40insG