Canonical Allele Identifier: CA2793087691

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178809_89178810insACA , CM000673.2:g.89178809_89178810insACA	GRCh38
NC_000011.9:g.88911977_88911978insACA , CM000673.1:g.88911977_88911978insACA	GRCh37
NC_000011.8:g.88551625_88551626insACA	NCBI36
NG_008748.1:g.5938_5939insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+37_819+38insACA MANE Select	ENSP00000263321.4:n.819+37_819+38insACA
ENST00000263321.5:c.819+37_819+38insACA	ENSP00000263321.4:n.819+37_819+38insACA
ENST00000526139.1:n.880+37_880+38insACA
NM_000372.4:c.819+37_819+38insACA	NP_000363.1:n.819+37_819+38insACA
XM_011542970.1:c.819+37_819+38insACA	XP_011541272.1:n.819+37_819+38insACA
XM_011542970.2:c.819+37_819+38insACA	XP_011541272.1:n.819+37_819+38insACA
XR_001748321.1:n.2718-65277_2718-65276insTGT
XR_001748322.1:n.2733-65277_2733-65276insTGT
NM_000372.5:c.819+37_819+38insACA MANE Select	NP_000363.1:n.819+37_819+38insACA