Canonical Allele Identifier: CA2793086008

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284575_89284739del , CM000673.2:g.89284575_89284739del	GRCh38
NC_000011.9:g.89017743_89017907del , CM000673.1:g.89017743_89017907del	GRCh37
NC_000011.8:g.88657391_88657555del	NCBI36
NG_008748.1:g.111704_111868del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1185-198_1185-34del MANE Select	ENSP00000263321.4:n.1185-198_1185-34del
ENST00000263321.5:c.1185-198_1185-34del	ENSP00000263321.4:n.1185-198_1185-34del
ENST00000528243.1:n.183-198_183-34del
NM_000372.4:c.1185-198_1185-34del	NP_000363.1:n.1185-198_1185-34del
XM_011542970.1:c.1185-198_1185-34del	XP_011541272.1:n.1185-198_1185-34del
XM_011542970.2:c.1185-198_1185-34del	XP_011541272.1:n.1185-198_1185-34del
XR_001748321.1:n.2456+1301_2456+1465del
XR_001748322.1:n.2457+1301_2457+1465del
NM_000372.5:c.1185-198_1185-34del MANE Select	NP_000363.1:n.1185-198_1185-34del