Canonical Allele Identifier: CA2793087711

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178834_89178835insAGA , CM000673.2:g.89178834_89178835insAGA	GRCh38
NC_000011.9:g.88912002_88912003insAGA , CM000673.1:g.88912002_88912003insAGA	GRCh37
NC_000011.8:g.88551650_88551651insAGA	NCBI36
NG_008748.1:g.5963_5964insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+62_819+63insAGA MANE Select	ENSP00000263321.4:n.819+62_819+63insAGA
ENST00000263321.5:c.819+62_819+63insAGA	ENSP00000263321.4:n.819+62_819+63insAGA
ENST00000526139.1:n.880+62_880+63insAGA
NM_000372.4:c.819+62_819+63insAGA	NP_000363.1:n.819+62_819+63insAGA
XM_011542970.1:c.819+62_819+63insAGA	XP_011541272.1:n.819+62_819+63insAGA
XM_011542970.2:c.819+62_819+63insAGA	XP_011541272.1:n.819+62_819+63insAGA
XR_001748321.1:n.2718-65302_2718-65301insTCT
XR_001748322.1:n.2733-65302_2733-65301insTCT
NM_000372.5:c.819+62_819+63insAGA MANE Select	NP_000363.1:n.819+62_819+63insAGA