Canonical Allele Identifier: CA2793087688

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178809_89178823del , CM000673.2:g.89178809_89178823del	GRCh38
NC_000011.9:g.88911977_88911991del , CM000673.1:g.88911977_88911991del	GRCh37
NC_000011.8:g.88551625_88551639del	NCBI36
NG_008748.1:g.5938_5952del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+37_819+51del MANE Select	ENSP00000263321.4:n.819+37_819+51del
ENST00000263321.5:c.819+37_819+51del	ENSP00000263321.4:n.819+37_819+51del
ENST00000526139.1:n.880+37_880+51del
NM_000372.4:c.819+37_819+51del	NP_000363.1:n.819+37_819+51del
XM_011542970.1:c.819+37_819+51del	XP_011541272.1:n.819+37_819+51del
XM_011542970.2:c.819+37_819+51del	XP_011541272.1:n.819+37_819+51del
XR_001748321.1:n.2718-65290_2718-65276del
XR_001748322.1:n.2733-65290_2733-65276del
NM_000372.5:c.819+37_819+51del MANE Select	NP_000363.1:n.819+37_819+51del