Canonical Allele Identifier: CA1989972732

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285211_89285212delinsGA , CM000673.2:g.89285211_89285212delinsGA	GRCh38
NC_000011.9:g.89018379_89018380delinsGA , CM000673.1:g.89018379_89018380delinsGA	GRCh37
NC_000011.8:g.88658027_88658028delinsGA	NCBI36
NG_008748.1:g.112340_112341delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+257_1366+258delinsGA MANE Select	ENSP00000263321.4:n.1366+257_1366+258delinsGA
ENST00000263321.5:c.1366+257_1366+258delinsGA	ENSP00000263321.4:n.1366+257_1366+258delinsGA
ENST00000528243.1:n.364+257_364+258delinsGA
NM_000372.4:c.1366+257_1366+258delinsGA	NP_000363.1:n.1366+257_1366+258delinsGA
XM_011542970.1:c.1366+257_1366+258delinsGA	XP_011541272.1:n.1366+257_1366+258delinsGA
XM_011542970.2:c.1366+257_1366+258delinsGA	XP_011541272.1:n.1366+257_1366+258delinsGA
XR_001748321.1:n.2456+822_2456+823delinsTC
XR_001748322.1:n.2457+822_2457+823delinsTC
NM_000372.5:c.1366+257_1366+258delinsGA MANE Select	NP_000363.1:n.1366+257_1366+258delinsGA