Canonical Allele Identifier: CA226650346

Gene: TYR

Linked Data

• dbSNP Id: rs200845965
• MyVariant Identifiers: chr11:g.89017873_89017874insA (hg19) ; chr11:g.89284705_89284706insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284710dup , CM000673.2:g.89284710dup	GRCh38
NC_000011.9:g.89017878dup , CM000673.1:g.89017878dup	GRCh37
NC_000011.8:g.88657526dup	NCBI36
NG_008748.1:g.111839dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.1185-63dup MANE Select	ENSP00000263321.4:n.1185-63dup
ENST00000263321.5:c.1185-63dup	ENSP00000263321.4:n.1185-63dup
ENST00000528243.1:n.183-63dup
NM_000372.4:c.1185-63dup	NP_000363.1:n.1185-63dup
XM_011542970.1:c.1185-63dup	XP_011541272.1:n.1185-63dup
XM_011542970.2:c.1185-63dup	XP_011541272.1:n.1185-63dup
XR_001748321.1:n.2456+1328dup
XR_001748322.1:n.2457+1328dup
NM_000372.5:c.1185-63dup MANE Select	NP_000363.1:n.1185-63dup