Canonical Allele Identifier: CA2724839994

Gene: TYR

Linked Data

• dbSNP Id: rs2135324599

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285105_89285107del , CM000673.2:g.89285105_89285107del	GRCh38
NC_000011.9:g.89018273_89018275del , CM000673.1:g.89018273_89018275del	GRCh37
NC_000011.8:g.88657921_88657923del	NCBI36
NG_008748.1:g.112234_112236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+151_1366+153del MANE Select	ENSP00000263321.4:n.1366+151_1366+153del
ENST00000263321.5:c.1366+151_1366+153del	ENSP00000263321.4:n.1366+151_1366+153del
ENST00000528243.1:n.364+151_364+153del
NM_000372.4:c.1366+151_1366+153del	NP_000363.1:n.1366+151_1366+153del
XM_011542970.1:c.1366+151_1366+153del	XP_011541272.1:n.1366+151_1366+153del
XM_011542970.2:c.1366+151_1366+153del	XP_011541272.1:n.1366+151_1366+153del
XR_001748321.1:n.2456+931_2456+933del
XR_001748322.1:n.2457+931_2457+933del
NM_000372.5:c.1366+151_1366+153del MANE Select	NP_000363.1:n.1366+151_1366+153del