Canonical Allele Identifier: CA2793086074

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285049_89285050insAGA , CM000673.2:g.89285049_89285050insAGA	GRCh38
NC_000011.9:g.89018217_89018218insAGA , CM000673.1:g.89018217_89018218insAGA	GRCh37
NC_000011.8:g.88657865_88657866insAGA	NCBI36
NG_008748.1:g.112178_112179insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+95_1366+96insAGA MANE Select	ENSP00000263321.4:n.1366+95_1366+96insAGA
ENST00000263321.5:c.1366+95_1366+96insAGA	ENSP00000263321.4:n.1366+95_1366+96insAGA
ENST00000528243.1:n.364+95_364+96insAGA
NM_000372.4:c.1366+95_1366+96insAGA	NP_000363.1:n.1366+95_1366+96insAGA
XM_011542970.1:c.1366+95_1366+96insAGA	XP_011541272.1:n.1366+95_1366+96insAGA
XM_011542970.2:c.1366+95_1366+96insAGA	XP_011541272.1:n.1366+95_1366+96insAGA
XR_001748321.1:n.2456+984_2456+985insTCT
XR_001748322.1:n.2457+984_2457+985insTCT
NM_000372.5:c.1366+95_1366+96insAGA MANE Select	NP_000363.1:n.1366+95_1366+96insAGA