Canonical Allele Identifier: CA2793087786

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178909_89178910insAGA , CM000673.2:g.89178909_89178910insAGA	GRCh38
NC_000011.9:g.88912077_88912078insAGA , CM000673.1:g.88912077_88912078insAGA	GRCh37
NC_000011.8:g.88551725_88551726insAGA	NCBI36
NG_008748.1:g.6038_6039insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+137_819+138insAGA MANE Select	ENSP00000263321.4:n.819+137_819+138insAGA
ENST00000263321.5:c.819+137_819+138insAGA	ENSP00000263321.4:n.819+137_819+138insAGA
ENST00000526139.1:n.880+137_880+138insAGA
NM_000372.4:c.819+137_819+138insAGA	NP_000363.1:n.819+137_819+138insAGA
XM_011542970.1:c.819+137_819+138insAGA	XP_011541272.1:n.819+137_819+138insAGA
XM_011542970.2:c.819+137_819+138insAGA	XP_011541272.1:n.819+137_819+138insAGA
XR_001748321.1:n.2718-65377_2718-65376insTCT
XR_001748322.1:n.2733-65377_2733-65376insTCT
NM_000372.5:c.819+137_819+138insAGA MANE Select	NP_000363.1:n.819+137_819+138insAGA