Canonical Allele Identifier: CA1989972619

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285138G= , CM000673.2:g.89285138G=	GRCh38
NC_000011.9:g.89018306G= , CM000673.1:g.89018306G=	GRCh37
NC_000011.8:g.88657954G=	NCBI36
NG_008748.1:g.112267G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+184G= MANE Select	ENSP00000263321.4:n.1366+184G=
ENST00000263321.5:c.1366+184G=	ENSP00000263321.4:n.1366+184G=
ENST00000528243.1:n.364+184G=
NM_000372.4:c.1366+184G=	NP_000363.1:n.1366+184G=
XM_011542970.1:c.1366+184G=	XP_011541272.1:n.1366+184G=
XM_011542970.2:c.1366+184G=	XP_011541272.1:n.1366+184G=
XR_001748321.1:n.2456+896C=
XR_001748322.1:n.2457+896C=
NM_000372.5:c.1366+184G= MANE Select	NP_000363.1:n.1366+184G=