Canonical Allele Identifier: CA2793086019

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284971_89284972insAC , CM000673.2:g.89284971_89284972insAC	GRCh38
NC_000011.9:g.89018139_89018140insAC , CM000673.1:g.89018139_89018140insAC	GRCh37
NC_000011.8:g.88657787_88657788insAC	NCBI36
NG_008748.1:g.112100_112101insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+17_1366+18insAC MANE Select	ENSP00000263321.4:n.1366+17_1366+18insAC
ENST00000263321.5:c.1366+17_1366+18insAC	ENSP00000263321.4:n.1366+17_1366+18insAC
ENST00000528243.1:n.364+17_364+18insAC
NM_000372.4:c.1366+17_1366+18insAC	NP_000363.1:n.1366+17_1366+18insAC
XM_011542970.1:c.1366+17_1366+18insAC	XP_011541272.1:n.1366+17_1366+18insAC
XM_011542970.2:c.1366+17_1366+18insAC	XP_011541272.1:n.1366+17_1366+18insAC
XR_001748321.1:n.2456+1062_2456+1063insGT
XR_001748322.1:n.2457+1062_2457+1063insGT
NM_000372.5:c.1366+17_1366+18insAC MANE Select	NP_000363.1:n.1366+17_1366+18insAC