Canonical Allele Identifier: CA1989972621

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285142_89285143delinsTG , CM000673.2:g.89285142_89285143delinsTG	GRCh38
NC_000011.9:g.89018310_89018311delinsTG , CM000673.1:g.89018310_89018311delinsTG	GRCh37
NC_000011.8:g.88657958_88657959delinsTG	NCBI36
NG_008748.1:g.112271_112272delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+188_1366+189delinsTG MANE Select	ENSP00000263321.4:n.1366+188_1366+189delinsTG
ENST00000263321.5:c.1366+188_1366+189delinsTG	ENSP00000263321.4:n.1366+188_1366+189delinsTG
ENST00000528243.1:n.364+188_364+189delinsTG
NM_000372.4:c.1366+188_1366+189delinsTG	NP_000363.1:n.1366+188_1366+189delinsTG
XM_011542970.1:c.1366+188_1366+189delinsTG	XP_011541272.1:n.1366+188_1366+189delinsTG
XM_011542970.2:c.1366+188_1366+189delinsTG	XP_011541272.1:n.1366+188_1366+189delinsTG
XR_001748321.1:n.2456+891_2456+892delinsCA
XR_001748322.1:n.2457+891_2457+892delinsCA
NM_000372.5:c.1366+188_1366+189delinsTG MANE Select	NP_000363.1:n.1366+188_1366+189delinsTG