Canonical Allele Identifier: CA2793087738

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178869_89178870insCAG , CM000673.2:g.89178869_89178870insCAG	GRCh38
NC_000011.9:g.88912037_88912038insCAG , CM000673.1:g.88912037_88912038insCAG	GRCh37
NC_000011.8:g.88551685_88551686insCAG	NCBI36
NG_008748.1:g.5998_5999insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+97_819+98insCAG MANE Select	ENSP00000263321.4:n.819+97_819+98insCAG
ENST00000263321.5:c.819+97_819+98insCAG	ENSP00000263321.4:n.819+97_819+98insCAG
ENST00000526139.1:n.880+97_880+98insCAG
NM_000372.4:c.819+97_819+98insCAG	NP_000363.1:n.819+97_819+98insCAG
XM_011542970.1:c.819+97_819+98insCAG	XP_011541272.1:n.819+97_819+98insCAG
XM_011542970.2:c.819+97_819+98insCAG	XP_011541272.1:n.819+97_819+98insCAG
XR_001748321.1:n.2718-65337_2718-65336insCTG
XR_001748322.1:n.2733-65337_2733-65336insCTG
NM_000372.5:c.819+97_819+98insCAG MANE Select	NP_000363.1:n.819+97_819+98insCAG