Canonical Allele Identifier: CA2793086092

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285073_89285074insACA , CM000673.2:g.89285073_89285074insACA	GRCh38
NC_000011.9:g.89018241_89018242insACA , CM000673.1:g.89018241_89018242insACA	GRCh37
NC_000011.8:g.88657889_88657890insACA	NCBI36
NG_008748.1:g.112202_112203insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+119_1366+120insACA MANE Select	ENSP00000263321.4:n.1366+119_1366+120insACA
ENST00000263321.5:c.1366+119_1366+120insACA	ENSP00000263321.4:n.1366+119_1366+120insACA
ENST00000528243.1:n.364+119_364+120insACA
NM_000372.4:c.1366+119_1366+120insACA	NP_000363.1:n.1366+119_1366+120insACA
XM_011542970.1:c.1366+119_1366+120insACA	XP_011541272.1:n.1366+119_1366+120insACA
XM_011542970.2:c.1366+119_1366+120insACA	XP_011541272.1:n.1366+119_1366+120insACA
XR_001748321.1:n.2456+960_2456+961insTGT
XR_001748322.1:n.2457+960_2457+961insTGT
NM_000372.5:c.1366+119_1366+120insACA MANE Select	NP_000363.1:n.1366+119_1366+120insACA