Canonical Allele Identifier: CA2793086095

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285080_89285081insG , CM000673.2:g.89285080_89285081insG	GRCh38
NC_000011.9:g.89018248_89018249insG , CM000673.1:g.89018248_89018249insG	GRCh37
NC_000011.8:g.88657896_88657897insG	NCBI36
NG_008748.1:g.112209_112210insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+126_1366+127insG MANE Select	ENSP00000263321.4:n.1366+126_1366+127insG
ENST00000263321.5:c.1366+126_1366+127insG	ENSP00000263321.4:n.1366+126_1366+127insG
ENST00000528243.1:n.364+126_364+127insG
NM_000372.4:c.1366+126_1366+127insG	NP_000363.1:n.1366+126_1366+127insG
XM_011542970.1:c.1366+126_1366+127insG	XP_011541272.1:n.1366+126_1366+127insG
XM_011542970.2:c.1366+126_1366+127insG	XP_011541272.1:n.1366+126_1366+127insG
XR_001748321.1:n.2456+953_2456+954insC
XR_001748322.1:n.2457+953_2457+954insC
NM_000372.5:c.1366+126_1366+127insG MANE Select	NP_000363.1:n.1366+126_1366+127insG