Canonical Allele Identifier: CA2793087729

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178856_89178857del , CM000673.2:g.89178856_89178857del	GRCh38
NC_000011.9:g.88912024_88912025del , CM000673.1:g.88912024_88912025del	GRCh37
NC_000011.8:g.88551672_88551673del	NCBI36
NG_008748.1:g.5985_5986del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+84_819+85del MANE Select	ENSP00000263321.4:n.819+84_819+85del
ENST00000263321.5:c.819+84_819+85del	ENSP00000263321.4:n.819+84_819+85del
ENST00000526139.1:n.880+84_880+85del
NM_000372.4:c.819+84_819+85del	NP_000363.1:n.819+84_819+85del
XM_011542970.1:c.819+84_819+85del	XP_011541272.1:n.819+84_819+85del
XM_011542970.2:c.819+84_819+85del	XP_011541272.1:n.819+84_819+85del
XR_001748321.1:n.2718-65324_2718-65323del
XR_001748322.1:n.2733-65324_2733-65323del
NM_000372.5:c.819+84_819+85del MANE Select	NP_000363.1:n.819+84_819+85del