Canonical Allele Identifier: CA2793086020

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284974_89284975insACTG , CM000673.2:g.89284974_89284975insACTG	GRCh38
NC_000011.9:g.89018142_89018143insACTG , CM000673.1:g.89018142_89018143insACTG	GRCh37
NC_000011.8:g.88657790_88657791insACTG	NCBI36
NG_008748.1:g.112103_112104insACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+20_1366+21insACTG MANE Select	ENSP00000263321.4:n.1366+20_1366+21insACTG
ENST00000263321.5:c.1366+20_1366+21insACTG	ENSP00000263321.4:n.1366+20_1366+21insACTG
ENST00000528243.1:n.364+20_364+21insACTG
NM_000372.4:c.1366+20_1366+21insACTG	NP_000363.1:n.1366+20_1366+21insACTG
XM_011542970.1:c.1366+20_1366+21insACTG	XP_011541272.1:n.1366+20_1366+21insACTG
XM_011542970.2:c.1366+20_1366+21insACTG	XP_011541272.1:n.1366+20_1366+21insACTG
XR_001748321.1:n.2456+1059_2456+1060insCAGT
XR_001748322.1:n.2457+1059_2457+1060insCAGT
NM_000372.5:c.1366+20_1366+21insACTG MANE Select	NP_000363.1:n.1366+20_1366+21insACTG