Canonical Allele Identifier: CA2793087749

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178875_89178884del , CM000673.2:g.89178875_89178884del	GRCh38
NC_000011.9:g.88912043_88912052del , CM000673.1:g.88912043_88912052del	GRCh37
NC_000011.8:g.88551691_88551700del	NCBI36
NG_008748.1:g.6004_6013del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+103_819+112del MANE Select	ENSP00000263321.4:n.819+103_819+112del
ENST00000263321.5:c.819+103_819+112del	ENSP00000263321.4:n.819+103_819+112del
ENST00000526139.1:n.880+103_880+112del
NM_000372.4:c.819+103_819+112del	NP_000363.1:n.819+103_819+112del
XM_011542970.1:c.819+103_819+112del	XP_011541272.1:n.819+103_819+112del
XM_011542970.2:c.819+103_819+112del	XP_011541272.1:n.819+103_819+112del
XR_001748321.1:n.2718-65350_2718-65341del
XR_001748322.1:n.2733-65350_2733-65341del
NM_000372.5:c.819+103_819+112del MANE Select	NP_000363.1:n.819+103_819+112del