Canonical Allele Identifier: CA2793086104

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285099_89285100insAC , CM000673.2:g.89285099_89285100insAC	GRCh38
NC_000011.9:g.89018267_89018268insAC , CM000673.1:g.89018267_89018268insAC	GRCh37
NC_000011.8:g.88657915_88657916insAC	NCBI36
NG_008748.1:g.112228_112229insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+145_1366+146insAC MANE Select	ENSP00000263321.4:n.1366+145_1366+146insAC
ENST00000263321.5:c.1366+145_1366+146insAC	ENSP00000263321.4:n.1366+145_1366+146insAC
ENST00000528243.1:n.364+145_364+146insAC
NM_000372.4:c.1366+145_1366+146insAC	NP_000363.1:n.1366+145_1366+146insAC
XM_011542970.1:c.1366+145_1366+146insAC	XP_011541272.1:n.1366+145_1366+146insAC
XM_011542970.2:c.1366+145_1366+146insAC	XP_011541272.1:n.1366+145_1366+146insAC
XR_001748321.1:n.2456+934_2456+935insGT
XR_001748322.1:n.2457+934_2457+935insGT
NM_000372.5:c.1366+145_1366+146insAC MANE Select	NP_000363.1:n.1366+145_1366+146insAC