Canonical Allele Identifier: CA2793086057

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285024_89285025insACAC , CM000673.2:g.89285024_89285025insACAC	GRCh38
NC_000011.9:g.89018192_89018193insACAC , CM000673.1:g.89018192_89018193insACAC	GRCh37
NC_000011.8:g.88657840_88657841insACAC	NCBI36
NG_008748.1:g.112153_112154insACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+70_1366+71insACAC MANE Select	ENSP00000263321.4:n.1366+70_1366+71insACAC
ENST00000263321.5:c.1366+70_1366+71insACAC	ENSP00000263321.4:n.1366+70_1366+71insACAC
ENST00000528243.1:n.364+70_364+71insACAC
NM_000372.4:c.1366+70_1366+71insACAC	NP_000363.1:n.1366+70_1366+71insACAC
XM_011542970.1:c.1366+70_1366+71insACAC	XP_011541272.1:n.1366+70_1366+71insACAC
XM_011542970.2:c.1366+70_1366+71insACAC	XP_011541272.1:n.1366+70_1366+71insACAC
XR_001748321.1:n.2456+1009_2456+1010insGTGT
XR_001748322.1:n.2457+1009_2457+1010insGTGT
NM_000372.5:c.1366+70_1366+71insACAC MANE Select	NP_000363.1:n.1366+70_1366+71insACAC