Canonical Allele Identifier: CA2615484144

Gene: TYR

Linked Data

• gnomAD v4: 11-89284705-TA-T

Genomic Alleles

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

Transcript Alleles

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