Canonical Allele Identifier: CA2793087784

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178908_89178909insACC , CM000673.2:g.89178908_89178909insACC	GRCh38
NC_000011.9:g.88912076_88912077insACC , CM000673.1:g.88912076_88912077insACC	GRCh37
NC_000011.8:g.88551724_88551725insACC	NCBI36
NG_008748.1:g.6037_6038insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+136_819+137insACC MANE Select	ENSP00000263321.4:n.819+136_819+137insACC
ENST00000263321.5:c.819+136_819+137insACC	ENSP00000263321.4:n.819+136_819+137insACC
ENST00000526139.1:n.880+136_880+137insACC
NM_000372.4:c.819+136_819+137insACC	NP_000363.1:n.819+136_819+137insACC
XM_011542970.1:c.819+136_819+137insACC	XP_011541272.1:n.819+136_819+137insACC
XM_011542970.2:c.819+136_819+137insACC	XP_011541272.1:n.819+136_819+137insACC
XR_001748321.1:n.2718-65376_2718-65375insGGT
XR_001748322.1:n.2733-65376_2733-65375insGGT
NM_000372.5:c.819+136_819+137insACC MANE Select	NP_000363.1:n.819+136_819+137insACC