Canonical Allele Identifier: CA2543576040

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285206A>G , CM000673.2:g.89285206A>G	GRCh38
NC_000011.9:g.89018374A>G , CM000673.1:g.89018374A>G	GRCh37
NC_000011.8:g.88658022A>G	NCBI36
NG_008748.1:g.112335A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+252A>G MANE Select	ENSP00000263321.4:n.1366+252A>G
ENST00000263321.5:c.1366+252A>G	ENSP00000263321.4:n.1366+252A>G
ENST00000528243.1:n.364+252A>G
NM_000372.4:c.1366+252A>G	NP_000363.1:n.1366+252A>G
XM_011542970.1:c.1366+252A>G	XP_011541272.1:n.1366+252A>G
XM_011542970.2:c.1366+252A>G	XP_011541272.1:n.1366+252A>G
XR_001748321.1:n.2456+828T>C
XR_001748322.1:n.2457+828T>C
NM_000372.5:c.1366+252A>G MANE Select	NP_000363.1:n.1366+252A>G