Canonical Allele Identifier: CA2793086076

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285051_89285052del , CM000673.2:g.89285051_89285052del	GRCh38
NC_000011.9:g.89018219_89018220del , CM000673.1:g.89018219_89018220del	GRCh37
NC_000011.8:g.88657867_88657868del	NCBI36
NG_008748.1:g.112180_112181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+97_1366+98del MANE Select	ENSP00000263321.4:n.1366+97_1366+98del
ENST00000263321.5:c.1366+97_1366+98del	ENSP00000263321.4:n.1366+97_1366+98del
ENST00000528243.1:n.364+97_364+98del
NM_000372.4:c.1366+97_1366+98del	NP_000363.1:n.1366+97_1366+98del
XM_011542970.1:c.1366+97_1366+98del	XP_011541272.1:n.1366+97_1366+98del
XM_011542970.2:c.1366+97_1366+98del	XP_011541272.1:n.1366+97_1366+98del
XR_001748321.1:n.2456+982_2456+983del
XR_001748322.1:n.2457+982_2457+983del
NM_000372.5:c.1366+97_1366+98del MANE Select	NP_000363.1:n.1366+97_1366+98del